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nsv5475180

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 20 studies. See in: genome view    
Submitted genomic117,596,740-117,596,884Question Mark
Overlapping variant regions from other studies: 140 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):117,236,794-117,236,938Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5475180Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7117,596,740117,596,884
nsv5475180RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7117,236,794117,236,938

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001692deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001692Submitted genomicNC_000007.14:g.117
596740_117596884de
l
GRCh38 (hg38)NC_000007.14Chr7117,596,740117,596,884
nssv17001692RemappedPerfectNC_000007.13:g.117
236794_117236938de
l
GRCh37.p13First PassNC_000007.13Chr7117,236,794117,236,938

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)
nssv17001692<0.00116404
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