A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525859



Internal ID15453152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128928389..129056403hg38UCSC Ensembl
InnerchrX:128062367..128190380hg19UCSC Ensembl
InnerchrX:127890048..128018061hg18UCSC Ensembl
InnerchrX:127787902..127915915hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38128015
hg19128014
hg18128014
hg17128014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702055
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525859
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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