A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066657



Internal ID18809188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32498083..32578496hg38UCSC Ensembl
Innerchr21:33870393..33950806hg19UCSC Ensembl
Innerchr21:32792264..32872677hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3880414
hg1980414
hg1880414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600130
Samples
Known GenesEVA1C, TCP10L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066657
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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