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nsv4050814

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:829,406

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 584 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):44,007,930-44,837,335Question Mark
Overlapping variant regions from other studies: 584 SVs from 20 studies. See in: genome view    
Submitted genomic44,473,602-45,303,007Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4050814RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr144,007,93044,837,335
nsv4050814Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr144,473,60245,303,007

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15961187duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15961187RemappedPerfectNC_000001.11:g.440
07930_44837335dup
GRCh38.p12First PassNC_000001.11Chr144,007,93044,837,335
nssv15961187Submitted genomicNC_000001.10:g.444
73602_45303007dup
GRCh37.p13NC_000001.10Chr144,473,60245,303,007

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)
nssv159611874.6e-005121694
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