A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967742



Internal ID18602970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:47705742..47707541hg38UCSC Ensembl
Innerchr4:47707759..47709558hg19UCSC Ensembl
Innerchr4:47402516..47404315hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381800
hg191800
hg181800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2318384, nssv2318386, nssv2318380, nssv2318378, nssv2318382, nssv2318383, nssv2318377, nssv2318385, nssv2318381, nssv2318379
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCORIN
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967742
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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