A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968690



Internal ID18603918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63776356..63918447hg38UCSC Ensembl
Innerchr9:68372090..68514181hg19UCSC Ensembl
Innerchr9:67861910..68004058hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38142092
hg19142092
hg18142149
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2549929, nssv2549922, nssv2549923, nssv2549931, nssv2549927, nssv2549925, nssv2549928, nssv2549930, nssv2549926, nssv2549924
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC642236
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968690
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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