A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963818



Internal ID18599058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:94838374..94840054hg38UCSC Ensembl
Innerchr2:95504119..95505799hg19UCSC Ensembl
Innerchr2:94867846..94869526hg18UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg381681
hg191681
hg181681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2667794, nssv2667797, nssv2667796, nssv2667793, nssv2667791, nssv2667798, nssv2667795, nssv2667792, nssv2667789, nssv2667790
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A8P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963818
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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