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nsv4204018

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,364

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 41 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):56,209,093-56,232,456Question Mark
Overlapping variant regions from other studies: 41 SVs from 10 studies. See in: genome view    
Submitted genomic56,602,877-56,626,240Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4204018RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1256,209,09356,232,456
nsv4204018Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1256,602,87756,626,240

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15953165duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15953165RemappedPerfectNC_000012.12:g.562
09093_56232456dup
GRCh38.p12First PassNC_000012.12Chr1256,209,09356,232,456
nssv15953165Submitted genomicNC_000012.11:g.566
02877_56626240dup
GRCh37.p13NC_000012.11Chr1256,602,87756,626,240

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)
nssv159531654.6e-005121694
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