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nsv4519695

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,347,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 802 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):85,661,876-87,008,877Question Mark
Overlapping variant regions from other studies: 802 SVs from 19 studies. See in: genome view    
Submitted genomic85,888,999-87,236,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4519695RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr285,661,87687,008,877
nsv4519695Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr285,888,99987,236,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15871781deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15871781RemappedPerfectNC_000002.12:g.856
61876_87008877del
GRCh38.p12First PassNC_000002.12Chr285,661,87687,008,877
nssv15871781Submitted genomicNC_000002.11:g.858
88999_87236000del
GRCh37.p13NC_000002.11Chr285,888,99987,236,000

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)
nssv158717814.6e-005121640
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