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nsv4517517

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111,012

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 271 SVs from 14 studies. See in: genome view    
Remapped(Score: Good):141,086,814-141,197,825Question Mark
Overlapping variant regions from other studies: 270 SVs from 14 studies. See in: genome view    
Submitted genomic140,180,999-140,292,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4517517RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX141,086,814141,197,825
nsv4517517Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX140,180,999140,292,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15989396duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15989396RemappedGoodNC_000023.11:g.141
086814_141197825du
p
GRCh38.p12First PassNC_000023.11ChrX141,086,814141,197,825
nssv15989396Submitted genomicNC_000023.10:g.140
180999_140292000du
p
GRCh37.p13NC_000023.10ChrX140,180,999140,292,000

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)
nssv15989396<0.0012121694
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