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nsv4122452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113,073

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):36,972,908-37,085,980Question Mark
Overlapping variant regions from other studies: 130 SVs from 17 studies. See in: genome view    
Submitted genomic36,940,684-37,053,756Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4122452RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr636,972,90837,085,980
nsv4122452Submitted genomicGRCh37.p13Primary AssemblyNC_000006.11Chr636,940,68437,053,756

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15978406duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15978406RemappedPerfectNC_000006.12:g.369
72908_37085980dup
GRCh38.p12First PassNC_000006.12Chr636,972,90837,085,980
nssv15978406Submitted genomicNC_000006.11:g.369
40684_37053756dup
GRCh37.p13NC_000006.11Chr636,940,68437,053,756

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)
nssv159784064.6e-005121694
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