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nsv4069920

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,584

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 372 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):217,814,553-218,303,136Question Mark
Overlapping variant regions from other studies: 374 SVs from 19 studies. See in: genome view    
Submitted genomic217,987,895-218,476,478Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4069920RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1217,814,553218,303,136
nsv4069920Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1217,987,895218,476,478

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15964605duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15964605RemappedPerfectNC_000001.11:g.217
814553_218303136du
p
GRCh38.p12First PassNC_000001.11Chr1217,814,553218,303,136
nssv15964605Submitted genomicNC_000001.10:g.217
987895_218476478du
p
GRCh37.p13NC_000001.10Chr1217,987,895218,476,478

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)
nssv15964605<0.001321694
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