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nsv4517672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:71,852

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 209 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):107,940,269-108,012,120Question Mark
Overlapping variant regions from other studies: 209 SVs from 15 studies. See in: genome view    
Submitted genomic107,183,499-107,255,350Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4517672RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX107,940,269108,012,120
nsv4517672Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX107,183,499107,255,350

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15988714duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15988714RemappedPerfectNC_000023.11:g.107
940269_108012120du
p
GRCh38.p12First PassNC_000023.11ChrX107,940,269108,012,120
nssv15988714Submitted genomicNC_000023.10:g.107
183499_107255350du
p
GRCh37.p13NC_000023.10ChrX107,183,499107,255,350

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)
nssv15988714<0.001521694
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