A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980252



Internal ID18615452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:119069166..119070482hg38UCSC Ensembl
Innerchr4:119990321..119991637hg19UCSC Ensembl
Innerchr4:120209769..120211085hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381317
hg191317
hg181317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2334470, nssv2334473, nssv2334474, nssv2334475, nssv2334469, nssv2334472, nssv2334467, nssv2334466, nssv2334468, nssv2334471
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)nsv980252
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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