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nsv6182435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:286

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 32 studies. See in: genome view    
Submitted genomic112,391,401-112,391,686Question Mark
Overlapping variant regions from other studies: 138 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):112,031,456-112,031,741Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6182435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7112,391,401112,391,686
nsv6182435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7112,031,456112,031,741

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17891990deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17891990Submitted genomicNC_000007.14:g.112
391401_112391686de
l
GRCh38 (hg38)NC_000007.14Chr7112,391,401112,391,686
nssv17891990RemappedPerfectNC_000007.13:g.112
031456_112031741de
l
GRCh37.p13First PassNC_000007.13Chr7112,031,456112,031,741

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)
nssv178919900.0032696
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