A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973699



Internal ID18608914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67894703..67895203hg38UCSC Ensembl
Innerchr9:67962149..67962649hg19UCSC Ensembl
Innerchr9:67551969..67552469hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2741276, nssv2741267, nssv2741269, nssv2741268, nssv2741272, nssv2741270, nssv2741271, nssv2741274, nssv2741273, nssv2741275
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)nsv973699
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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