A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969659



Internal ID18604886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67897059..67898672hg38UCSC Ensembl
Innerchr9:67964505..67966118hg19UCSC Ensembl
Innerchr9:67554325..67555938hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381614
hg191614
hg181614
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2741453, nssv2742309, nssv2741451, nssv2742307, nssv2742312, nssv2741448, nssv2742308, nssv2742311, nssv2741454, nssv2742316, nssv2742314, nssv2741446, nssv2741445, nssv2741447, nssv2742313, nssv2742310, nssv2741449, nssv2741452, nssv2741450, nssv2742315
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A1, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969659
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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