A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973614



Internal ID18608829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64406835..64407781hg38UCSC Ensembl
Innerchr9:43095332..43096279hg19UCSC Ensembl
Innerchr9:43085328..43086275hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38947
hg19948
hg18948
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731136, nssv2731134, nssv2731137, nssv2731130, nssv2731138, nssv2731132, nssv2731129, nssv2731133, nssv2731135, nssv2731131
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973614
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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