A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528246



Internal ID15455539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15563569..15607720hg38UCSC Ensembl
Innerchr21:16935888..16980039hg19UCSC Ensembl
Innerchr21:15857759..15901910hg18UCSC Ensembl
Innerchr21:15857759..15901910hg17UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3844152
hg1944152
hg1844152
hg1744152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704810
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528246
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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