A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979432



Internal ID18614635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:36074243..36085756hg38UCSC Ensembl
Innerchr20:34662165..34673678hg19UCSC Ensembl
Innerchr20:34125579..34137092hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3811514
hg1911514
hg1811514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2236184, nssv2236191, nssv2236189, nssv2236187, nssv2236186, nssv2236190, nssv2236183, nssv2236192, nssv2236185, nssv2236188
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)nsv979432
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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