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nsv4101503

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:262

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 51 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):190,877,780-190,878,041Question Mark
Overlapping variant regions from other studies: 51 SVs from 6 studies. See in: genome view    
Submitted genomic190,595,569-190,595,830Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4101503RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3190,877,780190,878,041
nsv4101503Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3190,595,569190,595,830

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15889217deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15889217RemappedPerfectNC_000003.12:g.190
877780_190878041de
l
GRCh38.p12First PassNC_000003.12Chr3190,877,780190,878,041
nssv15889217Submitted genomicNC_000003.11:g.190
595569_190595830de
l
GRCh37.p13NC_000003.11Chr3190,595,569190,595,830

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv158892174.6e-005121694
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