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nsv4069041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:707

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 34 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):68,127,921-68,128,627Question Mark
Overlapping variant regions from other studies: 34 SVs from 10 studies. See in: genome view    
Submitted genomic68,355,053-68,355,759Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4069041RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr268,127,92168,128,627
nsv4069041Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr268,355,05368,355,759

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15869372deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15869372RemappedPerfectNC_000002.12:g.681
27921_68128627del
GRCh38.p12First PassNC_000002.12Chr268,127,92168,128,627
nssv15869372Submitted genomicNC_000002.11:g.683
55053_68355759del
GRCh37.p13NC_000002.11Chr268,355,05368,355,759

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)
nssv15869372<0.001521694
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