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nsv5538574

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
Submitted genomic161,438,946-161,438,965Question Mark
Overlapping variant regions from other studies: 123 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):161,156,734-161,156,753Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538574Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3161,438,946161,438,965
nsv5538574RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3161,156,734161,156,753

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16940205insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16940205Submitted genomicNC_000003.12:g.161
438946_161438965in
s64
GRCh38 (hg38)NC_000003.12Chr3161,438,946161,438,965
nssv16940205RemappedPerfectNC_000003.11:g.161
156734_161156753in
s64
GRCh37.p13First PassNC_000003.11Chr3161,156,734161,156,753

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)
nssv169402050.074466372
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