A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976012



Internal ID18611219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81553716..81554899hg38UCSC Ensembl
Innerchr11:81264758..81265941hg19UCSC Ensembl
Innerchr11:80942406..80943589hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381184
hg191184
hg181184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2617945, nssv2618567, nssv2617944, nssv2618568, nssv2618564, nssv2618566, nssv2617946, nssv2618565, nssv2617943, nssv2617947
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)nsv976012
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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