A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962561



Internal ID18597804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21742826..21756255hg38UCSC Ensembl
Innerchr20:21723464..21736893hg19UCSC Ensembl
Innerchr20:21671464..21684893hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3813430
hg1913430
hg1813430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2232541, nssv2232543, nssv2232545, nssv2232542, nssv2232537, nssv2232536, nssv2232544, nssv2232540, nssv2232538, nssv2232539
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962561
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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