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nsv4077200

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,541

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 30 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):51,984,260-51,987,800Question Mark
Overlapping variant regions from other studies: 30 SVs from 6 studies. See in: genome view    
Submitted genomic52,018,276-52,021,816Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4077200RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr351,984,26051,987,800
nsv4077200Submitted genomicGRCh37.p13Primary AssemblyNC_000003.11Chr352,018,27652,021,816

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15877889deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15877889RemappedPerfectNC_000003.12:g.519
84260_51987800del
GRCh38.p12First PassNC_000003.12Chr351,984,26051,987,800
nssv15877889Submitted genomicNC_000003.11:g.520
18276_52021816del
GRCh37.p13NC_000003.11Chr352,018,27652,021,816

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)
nssv158778894.6e-005121694
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