A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964895



Internal ID18600131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:75910558..75912032hg38UCSC Ensembl
Innerchr5:75206383..75207857hg19UCSC Ensembl
Innerchr5:75242139..75243613hg18UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg381475
hg191475
hg181475
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2366086, nssv2366095, nssv2366092, nssv2366088, nssv2366090, nssv2366087, nssv2366091, nssv2366094, nssv2366089, nssv2366093
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)nsv964895
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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