A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966336



Internal ID18601566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165011672..165014562hg38UCSC Ensembl
Innerchr4:165932824..165935714hg19UCSC Ensembl
Innerchr4:166152274..166155164hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg382891
hg192891
hg182891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2340377, nssv2340380, nssv2340381, nssv2340378, nssv2340379, nssv2340382, nssv2340386, nssv2340384, nssv2340385, nssv2340383
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)nsv966336
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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