A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065706



Internal ID19154925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:23504968..23815616hg38UCSC Ensembl
Innerchr21:24877287..25187933hg19UCSC Ensembl
Innerchr21:23799158..24109804hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38310649
hg19310647
hg18310647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600069
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)nsv1065706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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