A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv964371



Internal ID18599609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4023748..4026726hg38UCSC Ensembl
Innerchr20:4004395..4007373hg19UCSC Ensembl
Innerchr20:3952395..3955373hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382979
hg192979
hg182979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2228096, nssv2228090, nssv2228089, nssv2228091, nssv2228095, nssv2228098, nssv2228093, nssv2228092, nssv2228094, nssv2228097
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)nsv964371
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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