A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967845



Internal ID18603073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:118658124..118667492hg38UCSC Ensembl
Innerchr4:119579279..119588647hg19UCSC Ensembl
Innerchr4:119798727..119808095hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg389369
hg199369
hg189369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2696056, nssv2696054, nssv2696057, nssv2696055, nssv2696050, nssv2696049, nssv2696058, nssv2696052, nssv2696051, nssv2696053
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967845
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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