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nsv4201396

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,073

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):4,560,919-4,669,991Question Mark
Overlapping variant regions from other studies: 123 SVs from 14 studies. See in: genome view    
Submitted genomic4,582,149-4,691,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4201396RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr114,560,9194,669,991
nsv4201396Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr114,582,1494,691,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15798128deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15798128RemappedPerfectNC_000011.10:g.456
0919_4669991del
GRCh38.p12First PassNC_000011.10Chr114,560,9194,669,991
nssv15798128Submitted genomicNC_000011.9:g.4582
149_4691221del
GRCh37.p13NC_000011.9Chr114,582,1494,691,221

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)
nssv157981284.6e-005121694
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