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nsv884849

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,316

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1793 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):32,486,077-32,500,392Question Mark
Overlapping variant regions from other studies: 1793 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):32,453,854-32,468,169Question Mark
Overlapping variant regions from other studies: 1193 SVs from 31 studies. See in: genome view    
Submitted genomic32,561,832-32,576,147Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv884849RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nsv884849RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nsv884849Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr632,561,83232,563,46032,574,20232,576,147

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1500817copy number lossSP50857SNP arraySNP genotyping analysis20
nssv1503300copy number lossSP52027SNP arraySNP genotyping analysis14
nssv1505453copy number lossSP53528SNP arraySNP genotyping analysis23
nssv1506390copy number lossSP54294SNP arraySNP genotyping analysis10
nssv1511654copy number lossSP55026SNP arraySNP genotyping analysis21
nssv1511772copy number lossSP55074SNP arraySNP genotyping analysis8
nssv1513132copy number lossSP55690SNP arraySNP genotyping analysis15
nssv1513212copy number lossSP55695SNP arraySNP genotyping analysis14
nssv1514781copy number lossSP56079SNP arraySNP genotyping analysis12
nssv1514946copy number lossSP56104SNP arraySNP genotyping analysis19
nssv1515104copy number lossSP56125SNP arraySNP genotyping analysis28
nssv1515153copy number lossSP56128SNP arraySNP genotyping analysis14
nssv1516066copy number lossSP56396SNP arraySNP genotyping analysis18
nssv1516264copy number lossSP56734SNP arraySNP genotyping analysis23
nssv1516660copy number lossSP56887SNP arraySNP genotyping analysis16
nssv1519468copy number lossSP81047SNP arraySNP genotyping analysis19

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1500817RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1503300RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1505453RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1506390RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1511654RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1511772RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1513132RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1513212RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1514781RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1514946RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1515104RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1515153RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1516066RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1516264RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1516660RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1519468RemappedPerfectNC_000006.12:g.(32
486077_32487705)_(
32498447_32500392)
del
GRCh38.p12First PassNC_000006.12Chr632,486,07732,487,70532,498,44732,500,392
nssv1500817RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1503300RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1505453RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1506390RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1511654RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1511772RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1513132RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1513212RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1514781RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1514946RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1515104RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1515153RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1516066RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1516264RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1516660RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1519468RemappedPerfectNC_000006.11:g.(32
453854_32455482)_(
32466224_32468169)
del
GRCh37.p13First PassNC_000006.11Chr632,453,85432,455,48232,466,22432,468,169
nssv1500817Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1503300Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1505453Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1506390Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1511654Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1511772Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1513132Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1513212Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1514781Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1514946Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1515104Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1515153Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1516066Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1516264Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1516660Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147
nssv1519468Submitted genomicNC_000006.10:g.(32
561832_32563460)_(
32574202_32576147)
del
NCBI36 (hg18)NC_000006.10Chr632,561,83232,563,46032,574,20232,576,147

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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