A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516175



Internal ID15443468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36126057..36245332hg38UCSC Ensembl
Innerchr21:37498355..37617630hg19UCSC Ensembl
Innerchr21:36420225..36539500hg18UCSC Ensembl
Innerchr21:36420225..36539500hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38119276
hg19119276
hg18119276
hg17119276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673570, nssv683841, nssv662382, nssv691047, nssv684079, nssv666629
Samples
Known GenesCBR3, CBR3-AS1, DOPEY2, LOC100133286
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516175
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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