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nsv5453393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
Submitted genomic125,028,027-125,028,094Question Mark
Overlapping variant regions from other studies: 111 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):124,746,871-124,746,938Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453393Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3125,028,027125,028,094
nsv5453393RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3124,746,871124,746,938

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16938166deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16938166Submitted genomicNC_000003.12:g.125
028027_125028094de
l
GRCh38 (hg38)NC_000003.12Chr3125,028,027125,028,094
nssv16938166RemappedPerfectNC_000003.11:g.124
746871_124746938de
l
GRCh37.p13First PassNC_000003.11Chr3124,746,871124,746,938

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)
nssv169381660.003186404
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