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nsv4053325

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,399

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 31 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):151,975,515-151,991,913Question Mark
Overlapping variant regions from other studies: 33 SVs from 10 studies. See in: genome view    
Submitted genomic151,947,991-151,964,389Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4053325RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1151,975,515151,991,913
nsv4053325Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1151,947,991151,964,389

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15963325duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15963325RemappedPerfectNC_000001.11:g.151
975515_151991913du
p
GRCh38.p12First PassNC_000001.11Chr1151,975,515151,991,913
nssv15963325Submitted genomicNC_000001.10:g.151
947991_151964389du
p
GRCh37.p13NC_000001.10Chr1151,947,991151,964,389

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)
nssv159633254.6e-005121694
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