A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963326



Internal ID18598567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63582649..63585407hg38UCSC Ensembl
Innerchr3:63568325..63571083hg19UCSC Ensembl
Innerchr3:63543365..63546123hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg382759
hg192759
hg182759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2284277, nssv2284282, nssv2284276, nssv2284275, nssv2284280, nssv2284273, nssv2284281, nssv2284274, nssv2284279, nssv2284278
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSYNPR
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963326
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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