A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973606



Internal ID18608821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65194067..65214345hg38UCSC Ensembl
Innerchr9:42788258..42808203hg19UCSC Ensembl
Innerchr9:42778254..42798199hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3820279
hg1919946
hg1819946
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2731419, nssv2731417, nssv2731425, nssv2731423, nssv2731421, nssv2731418, nssv2731420, nssv2731416, nssv2731422, nssv2731424
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)nsv973606
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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