A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964858



Internal ID18600094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:56503374..56506905hg38UCSC Ensembl
Innerchr5:55799201..55802732hg19UCSC Ensembl
Innerchr5:55834958..55838489hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg383532
hg193532
hg183532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2357233, nssv2357234, nssv2357225, nssv2357227, nssv2357232, nssv2357226, nssv2357229, nssv2357228, nssv2357231, nssv2357230
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)nsv964858
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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