A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060192



Internal ID19149411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:35742310..35920757hg38UCSC Ensembl
Innerchr21:37114608..37293055hg19UCSC Ensembl
Innerchr21:36036478..36214925hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38178448
hg19178448
hg18178448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732704
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060192
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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