A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972730



Internal ID18607946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62470876..62479911hg38UCSC Ensembl
Innerchr9:46782177..46791212hg19UCSC Ensembl
Innerchr9:46622173..46631208hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg389036
hg199036
hg189036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv90n82
Supporting Variantsnssv2543588, nssv2543587, nssv2543595, nssv2543589, nssv2543596, nssv2543592, nssv2543591, nssv2543594, nssv2543593, nssv2543590
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972730
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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