A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969667



Internal ID18604894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64387575..64390347hg38UCSC Ensembl
Innerchr9:69399993..69402765hg19UCSC Ensembl
Innerchr9:68689813..68692585hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382773
hg192773
hg182773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2744161, nssv2744158, nssv2744162, nssv2744154, nssv2744163, nssv2744157, nssv2744156, nssv2744159, nssv2744160, nssv2744155
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A4
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969667
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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