A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524313



Internal ID15451606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30974518..30990059hg38UCSC Ensembl
Innerchr21:32346837..32362378hg19UCSC Ensembl
Innerchr21:31268708..31284249hg18UCSC Ensembl
Innerchr21:31268708..31284249hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3815542
hg1915542
hg1815542
hg1715542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700215
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524313
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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