A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964911



Internal ID18600147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99495604..99521566hg38UCSC Ensembl
Innerchr5:98831308..98857270hg19UCSC Ensembl
Innerchr5:98859207..98885169hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3825963
hg1925963
hg1825963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2370364, nssv2370359, nssv2370358, nssv2370366, nssv2370357, nssv2370363, nssv2370361, nssv2370360, nssv2370362, nssv2370365
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)nsv964911
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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