A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668967



Internal ID15405619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121227596..121243278hg38UCSC Ensembl
InnerchrX:120361450..120377132hg19UCSC Ensembl
InnerchrX:120189131..120204813hg18UCSC Ensembl
InnerchrX:120086985..120102667hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3815683
hg1915683
hg1815683
hg1715683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517214
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668967
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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