A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964383



Internal ID18599621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:23922145..23924382hg38UCSC Ensembl
Innerchr20:23902782..23905019hg19UCSC Ensembl
Innerchr20:23850782..23853019hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg382238
hg192238
hg182238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2231160, nssv2231161, nssv2231157, nssv2231159, nssv2231156, nssv2231154, nssv2231155, nssv2231158, nssv2231162, nssv2231153
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv964383
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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