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nsv4047214

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:503,643

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 523 SVs from 18 studies. See in: genome view    
Remapped(Score: Good):144,491,973-144,995,615Question Mark
Overlapping variant regions from other studies: 519 SVs from 18 studies. See in: genome view    
Submitted genomic143,573,537-144,077,135Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4047214RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX144,491,973144,995,615
nsv4047214Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX143,573,537144,077,135

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15989446duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15989446RemappedGoodNC_000023.11:g.144
491973_144995615du
p
GRCh38.p12First PassNC_000023.11ChrX144,491,973144,995,615
nssv15989446Submitted genomicNC_000023.10:g.143
573537_144077135du
p
GRCh37.p13NC_000023.10ChrX143,573,537144,077,135

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)
nssv15989446<0.001421036
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