A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689387



Internal ID15426039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113898791..113958604hg38UCSC Ensembl
InnerchrX:113142068..113201889hg19UCSC Ensembl
InnerchrX:113028333..113088154hg18UCSC Ensembl
InnerchrX:112947822..113007643hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3859814
hg1959822
hg1859822
hg1759822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515718
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689387
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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