A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522615



Internal ID15449908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5558807..5590007hg38UCSC Ensembl
InnerchrX:5476848..5508048hg19UCSC Ensembl
InnerchrX:5486848..5518048hg18UCSC Ensembl
InnerchrX:5336584..5367784hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3831201
hg1931201
hg1831201
hg1731201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706010
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522615
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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