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nsv4532413

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:836

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 20 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):64,509,327-64,510,162Question Mark
Overlapping variant regions from other studies: 17 SVs from 4 studies. See in: genome view    
Submitted genomic62,505,445-62,506,280Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4532413RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1764,509,32764,510,162
nsv4532413Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1762,505,44562,506,280

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15834580deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15834580RemappedPerfectNC_000017.11:g.645
09327_64510162del
GRCh38.p12First PassNC_000017.11Chr1764,509,32764,510,162
nssv15834580Submitted genomicNC_000017.10:g.625
05445_62506280del
GRCh37.p13NC_000017.10Chr1762,505,44562,506,280

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)
nssv158345804.6e-005121646
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