A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967097



Internal ID18602326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182942862..182944897hg38UCSC Ensembl
Innerchr3:182660650..182662685hg19UCSC Ensembl
Innerchr3:184143344..184145379hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg382036
hg192036
hg182036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2304489, nssv2304484, nssv2304488, nssv2304483, nssv2304480, nssv2304487, nssv2304485, nssv2304486, nssv2304482, nssv2304481
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDCUN1D1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967097
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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