A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968707



Internal ID18603935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76543692..76549684hg38UCSC Ensembl
Innerchr9:79158608..79164600hg19UCSC Ensembl
Innerchr9:78348428..78354420hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385993
hg195993
hg185993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2554474, nssv2554477, nssv2554468, nssv2554472, nssv2554475, nssv2554470, nssv2554469, nssv2554471, nssv2554476, nssv2554473
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)nsv968707
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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