A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969636



Internal ID18604863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42913919..42921968hg38UCSC Ensembl
Innerchr9:66396588..66404638hg19UCSC Ensembl
Innerchr9:66136408..66144458hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg388050
hg198051
hg188051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737414, nssv2737405, nssv2737407, nssv2737406, nssv2737410, nssv2737409, nssv2737408, nssv2737411, nssv2737412, nssv2737413
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)nsv969636
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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