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nsv4573462

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 36 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):125,235,283-125,235,283Question Mark
Overlapping variant regions from other studies: 36 SVs from 5 studies. See in: genome view    
Submitted genomic124,954,127-124,954,127Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573462RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3125,235,283125,235,283
nsv4573462Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3124,954,127124,954,127

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16049860line1 insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16049860RemappedPerfectNC_000003.12:g.125
235283_125235284in
s2854
GRCh38.p12First PassNC_000003.12Chr3125,235,283125,235,283
nssv16049860Submitted genomicNC_000003.11:g.124
954127_124954128in
s2854
GRCh37.p13NC_000003.11Chr3124,954,127124,954,127

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)
nssv160498604.6e-005121694
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