A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528279



Internal ID15108886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41357910..41380411hg38UCSC Ensembl
Innerchr21:42729837..42752338hg19UCSC Ensembl
Innerchr21:41651707..41674208hg18UCSC Ensembl
Innerchr21:41651707..41674208hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3822502
hg1922502
hg1822502
hg1722502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704849
Samples
Known GenesMX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528279
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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