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nsv5537173

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 107 SVs from 23 studies. See in: genome view    
Submitted genomic125,034,195-125,034,243Question Mark
Overlapping variant regions from other studies: 107 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):124,753,039-124,753,087Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5537173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3125,034,195125,034,243
nsv5537173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3124,753,039124,753,087

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16938168insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16938168Submitted genomicNC_000003.12:g.125
034195_125034243in
s50
GRCh38 (hg38)NC_000003.12Chr3125,034,195125,034,243
nssv16938168RemappedPerfectNC_000003.11:g.124
753039_124753087in
s50
GRCh37.p13First PassNC_000003.11Chr3124,753,039124,753,087

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)
nssv169381680.43127636404
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