A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526774



Internal ID8421049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26082679..26090411hg38UCSC Ensembl
Innerchr21:27454995..27462727hg19UCSC Ensembl
Innerchr21:26376866..26384598hg18UCSC Ensembl
Innerchr21:26376866..26384598hg17UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg387733
hg197733
hg187733
hg177733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703126
Samples
Known GenesAPP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526774
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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