A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965874



Internal ID18601104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35850207..35851251hg38UCSC Ensembl
Innerchr20:34438129..34439173hg19UCSC Ensembl
Innerchr20:33901543..33902587hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381045
hg191045
hg181045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2234100, nssv2234097, nssv2234099, nssv2234095, nssv2234096, nssv2234101, nssv2234094, nssv2234103, nssv2234098, nssv2234102
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPHF20
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965874
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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