A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528966



Internal ID15456259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21856898..21885308hg38UCSC Ensembl
Innerchr2:22079770..22108180hg19UCSC Ensembl
Innerchr2:21933275..21961685hg18UCSC Ensembl
Innerchr2:21991422..22019832hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3828411
hg1928411
hg1828411
hg1728411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705665
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528966
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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