A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967789



Internal ID18603017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112787340..112789136hg38UCSC Ensembl
Innerchr4:113708496..113710292hg19UCSC Ensembl
Innerchr4:113927945..113929741hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381797
hg191797
hg181797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2331891, nssv2331893, nssv2331896, nssv2331892, nssv2331897, nssv2331898, nssv2331899, nssv2331895, nssv2331894, nssv2331900
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)nsv967789
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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