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nsv878052

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,312

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 167 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):183,972,477-184,002,788Question Mark
Overlapping variant regions from other studies: 167 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):183,690,265-183,720,576Question Mark
Overlapping variant regions from other studies: 60 SVs from 14 studies. See in: genome view    
Submitted genomic185,172,959-185,203,270Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv878052RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nsv878052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nsv878052Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1544577copy number lossMS16387SNP arraySNP genotyping analysis7
nssv1547489copy number lossMS17399SNP arraySNP genotyping analysis8
nssv1550614copy number lossMS18487SNP arraySNP genotyping analysis7
nssv1555898copy number lossMS21706SNP arraySNP genotyping analysis15
nssv1556248copy number lossMS21868SNP arraySNP genotyping analysis44
nssv1556678copy number lossMS22109SNP arraySNP genotyping analysis12
nssv1562718copy number lossMS25710SNP arraySNP genotyping analysis10
nssv1564038copy number lossIS30147SNP arraySNP genotyping analysis16
nssv1577821copy number lossIS34573SNP arraySNP genotyping analysis23
nssv1578950copy number lossIS34996SNP arraySNP genotyping analysis22
nssv1581706copy number lossIS35701SNP arraySNP genotyping analysis38
nssv1584413copy number lossIS36990SNP arraySNP genotyping analysis19
nssv1589632copy number lossIS38390SNP arraySNP genotyping analysis17
nssv1596557copy number lossIS40568SNP arraySNP genotyping analysis6
nssv1596836copy number lossIS40657SNP arraySNP genotyping analysis40
nssv1597067copy number lossIS40729SNP arraySNP genotyping analysis20
nssv1600266copy number lossIS41866SNP arraySNP genotyping analysis24

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1544577RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1547489RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1550614RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1555898RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1556248RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1556678RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1562718RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1564038RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1577821RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1578950RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1581706RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1584413RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1589632RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1596557RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1596836RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1597067RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1600266RemappedPerfectNC_000003.12:g.(18
3972477_183973663)
_(183996679_184002
788)del
GRCh38.p12First PassNC_000003.12Chr3183,972,477183,973,663183,996,679184,002,788
nssv1544577RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1547489RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1550614RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1555898RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1556248RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1556678RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1562718RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1564038RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1577821RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1578950RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1581706RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1584413RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1589632RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1596557RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1596836RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1597067RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1600266RemappedPerfectNC_000003.11:g.(18
3690265_183691451)
_(183714467_183720
576)del
GRCh37.p13First PassNC_000003.11Chr3183,690,265183,691,451183,714,467183,720,576
nssv1544577Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1547489Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1550614Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1555898Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1556248Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1556678Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1562718Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1564038Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1577821Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1578950Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1581706Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1584413Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1589632Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1596557Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1596836Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1597067Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270
nssv1600266Submitted genomicNC_000003.10:g.(18
5172959_185174145)
_(185197161_185203
270)del
NCBI36 (hg18)NC_000003.10Chr3185,172,959185,174,145185,197,161185,203,270

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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