A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968703



Internal ID18603931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68610800..68611300hg38UCSC Ensembl
Innerchr9:71225716..71226216hg19UCSC Ensembl
Innerchr9:70415536..70416036hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552214, nssv2550390, nssv2550391, nssv2550387, nssv2550388, nssv2552215, nssv2550392, nssv2550393, nssv2550389, nssv2552216
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)nsv968703
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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