A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972063



Internal ID18607279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95025598..95026598hg38UCSC Ensembl
Innerchr11:94758762..94759762hg19UCSC Ensembl
Innerchr11:94398410..94399410hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1903106, nssv1903110, nssv1903109, nssv1903111, nssv1903103, nssv1903108, nssv1903104, nssv1903107, nssv1903105, nssv1903112
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKDM4E
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972063
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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