A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685785



Internal ID15422437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113056323..113183439hg38UCSC Ensembl
InnerchrX:112299551..112426666hg19UCSC Ensembl
InnerchrX:112186207..112313322hg18UCSC Ensembl
InnerchrX:112105696..112232811hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38127117
hg19127116
hg18127116
hg17127116
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)nssv685785
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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