A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519860



Internal ID15447153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:84259442..84665655hg38UCSC Ensembl
InnerchrX:83514450..83920663hg19UCSC Ensembl
InnerchrX:83401106..83807319hg18UCSC Ensembl
InnerchrX:83320595..83726808hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38406214
hg19406214
hg18406214
hg17406214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697090
Samples
Known GenesHDX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519860
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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