A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965852



Internal ID18601082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7830978..7831847hg38UCSC Ensembl
Innerchr20:7811625..7812494hg19UCSC Ensembl
Innerchr20:7759625..7760494hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38870
hg19870
hg18870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2229358, nssv2228825, nssv2229357, nssv2229360, nssv2228827, nssv2228826, nssv2229359, nssv2229361, nssv2228824, nssv2229356
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)nsv965852
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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