A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975927



Internal ID18611134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56490385..56491385hg38UCSC Ensembl
Innerchr11:56257861..56258861hg19UCSC Ensembl
Innerchr11:56014437..56015437hg18UCSC Ensembl
Cytoband11q11
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 Variantsnssv1890150, nssv1890156, nssv1890155, nssv1890151, nssv1890148, nssv1890152, nssv1890154, nssv1889619, nssv1890153, nssv1890149
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR5M8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975927
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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