A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980194



Internal ID18615394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36433868..36444649hg38UCSC Ensembl
Innerchr4:36435490..36446271hg19UCSC Ensembl
Innerchr4:36111885..36122666hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3810782
hg1910782
hg1810782
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2316420, nssv2316417, nssv2316423, nssv2316416, nssv2316415, nssv2316421, nssv2316418, nssv2316422, nssv2316414, nssv2316419
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)nsv980194
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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