A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967003



Internal ID18602232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:36766788..36768813hg38UCSC Ensembl
Innerchr3:36808279..36810304hg19UCSC Ensembl
Innerchr3:36783283..36785308hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg382026
hg192026
hg182026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2277735, nssv2277737, nssv2277732, nssv2277740, nssv2277739, nssv2277734, nssv2277736, nssv2277733, nssv2277741, nssv2277738
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv967003
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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