A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969688



Internal ID18604915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65190773..65216788hg38UCSC Ensembl
Innerchr9:70084379..70110394hg19UCSC Ensembl
Innerchr9:69374199..69400214hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3826016
hg1926016
hg1826016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2752021, nssv2756023, nssv2748908, nssv2748754, nssv2753647, nssv2747850, nssv2750442, nssv2753956, nssv2753436, nssv2751441
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969688
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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