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nsv5486581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97,982

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 318 SVs from 48 studies. See in: genome view    
Submitted genomic107,567,980-107,665,961Question Mark
Overlapping variant regions from other studies: 318 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):107,208,425-107,306,406Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5486581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,567,980107,665,961
nsv5486581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,208,425107,306,406

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004036duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004036Submitted genomicNC_000007.14:g.107
567980_107665961du
p
GRCh38 (hg38)NC_000007.14Chr7107,567,980107,665,961
nssv17004036RemappedPerfectNC_000007.13:g.107
208425_107306406du
p
GRCh37.p13First PassNC_000007.13Chr7107,208,425107,306,406

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)
nssv17004036<0.00116404
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