A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526520



Internal ID15453813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:2897989..2898482hg38UCSC Ensembl
Innerchr2:2901761..2902254hg19UCSC Ensembl
Innerchr2:2880768..2881261hg18UCSC Ensembl
Innerchr2:2872058..2872551hg17UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38494
hg19494
hg18494
hg17494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702831
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526520
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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