A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665961



Internal ID15402613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113047245..113175125hg38UCSC Ensembl
InnerchrX:112290473..112418352hg19UCSC Ensembl
InnerchrX:112177129..112305008hg18UCSC Ensembl
InnerchrX:112096618..112224497hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38127881
hg19127880
hg18127880
hg17127880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515695
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665961
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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