A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967083



Internal ID18602312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161428617..161429805hg38UCSC Ensembl
Innerchr3:161146405..161147593hg19UCSC Ensembl
Innerchr3:162629099..162630287hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381189
hg191189
hg181189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2302066, nssv2302059, nssv2302061, nssv2302062, nssv2302063, nssv2302060, nssv2302065, nssv2302067, nssv2302064, nssv2302058
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC101243545
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967083
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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