A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980236



Internal ID18268750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102796375..102797470hg38UCSC Ensembl
Innerchr4:103717532..103718627hg19UCSC Ensembl
Innerchr4:103936616..103937711hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg381096
hg191096
hg181096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2330481, nssv2330474, nssv2330476, nssv2330479, nssv2330478, nssv2330477, nssv2330480, nssv2330475, nssv2330473, nssv2330482
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesUBE2D3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980236
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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