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nsv4057543

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:375,173

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 580 SVs from 20 studies. See in: genome view    
Remapped(Score: Pass):3,358,584-3,733,756Question Mark
Overlapping variant regions from other studies: 560 SVs from 20 studies. See in: genome view    
Submitted genomic3,362,355-3,781,346Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4057543RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr23,358,5843,733,756
nsv4057543Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr23,362,3553,781,346

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15968874duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15968874RemappedPassNC_000002.12:g.335
8584_3733756dup
GRCh38.p12First PassNC_000002.12Chr23,358,5843,733,756
nssv15968874Submitted genomicNC_000002.11:g.336
2355_3781346dup
GRCh37.p13NC_000002.11Chr23,362,3553,781,346

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)
nssv159688744.6e-005121694
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