A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966326



Internal ID18601556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:145133170..145138740hg38UCSC Ensembl
Innerchr4:146054322..146059892hg19UCSC Ensembl
Innerchr4:146273772..146279342hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg385571
hg195571
hg185571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2337296, nssv2337299, nssv2337293, nssv2337298, nssv2337294, nssv2337292, nssv2337300, nssv2337297, nssv2337301, nssv2337295
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOTUD4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966326
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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