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nsv4520648

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:499,502

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 315 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):154,808,210-155,307,711Question Mark
Overlapping variant regions from other studies: 315 SVs from 19 studies. See in: genome view    
Submitted genomic154,525,999-155,025,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4520648RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,808,210155,307,711
nsv4520648Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr3154,525,999155,025,500

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15883461deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15883461RemappedPerfectNC_000003.12:g.154
808210_155307711de
l
GRCh38.p12First PassNC_000003.12Chr3154,808,210155,307,711
nssv15883461Submitted genomicNC_000003.11:g.154
525999_155025500de
l
GRCh37.p13NC_000003.11Chr3154,525,999155,025,500

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)
nssv158834614.6e-005121694
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