A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965878



Internal ID18254422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45743778..45747966hg38UCSC Ensembl
Innerchr20:44372417..44376605hg19UCSC Ensembl
Innerchr20:43805824..43810012hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg384189
hg194189
hg184189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2238082, nssv2238075, nssv2238076, nssv2238077, nssv2238078, nssv2238080, nssv2238084, nssv2238079, nssv2238081, nssv2238083
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)nsv965878
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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