A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979815



Internal ID18615016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32259405..32260592hg38UCSC Ensembl
Innerchr3:32300897..32302084hg19UCSC Ensembl
Innerchr3:32275901..32277088hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381188
hg191188
hg181188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2274201, nssv2274205, nssv2274209, nssv2274210, nssv2274207, nssv2274206, nssv2274203, nssv2274204, nssv2274208, nssv2274202
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCMTM8
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979815
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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