A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963304



Internal ID18598545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27623427..27624442hg38UCSC Ensembl
Innerchr3:27664918..27665933hg19UCSC Ensembl
Innerchr3:27639922..27640937hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381016
hg191016
hg181016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2275451, nssv2275457, nssv2275456, nssv2275450, nssv2275452, nssv2275449, nssv2275453, nssv2275448, nssv2275454, nssv2275455
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)nsv963304
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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