A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965871



Internal ID18601101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34221753..34228435hg38UCSC Ensembl
Innerchr20:32809559..32816241hg19UCSC Ensembl
Innerchr20:32273220..32279902hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg386683
hg196683
hg186683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2235785, nssv2235782, nssv2235780, nssv2235783, nssv2235784, nssv2235786, nssv2235778, nssv2235779, nssv2235777, nssv2235781
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)nsv965871
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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