A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061075



Internal ID19150294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18744203..18836413hg38UCSC Ensembl
Innerchr21:20116521..20208731hg19UCSC Ensembl
Innerchr21:19038392..19130602hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3892211
hg1992211
hg1892211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599813
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)nsv1061075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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