A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964979



Internal ID18600214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177339457..177349330hg38UCSC Ensembl
Innerchr5:176766458..176776331hg19UCSC Ensembl
Innerchr5:176699064..176708937hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg389874
hg199874
hg189874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2388127, nssv2388119, nssv2388121, nssv2388122, nssv2388126, nssv2388118, nssv2388120, nssv2388124, nssv2388123, nssv2388125
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLMAN2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964979
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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