A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963365



Internal ID18598606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:142037735..142043914hg38UCSC Ensembl
Innerchr3:141756577..141762756hg19UCSC Ensembl
Innerchr3:143239267..143245446hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg386180
hg196180
hg186180
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2298180, nssv2298179, nssv2298174, nssv2298182, nssv2298183, nssv2298178, nssv2298177, nssv2298175, nssv2298176, nssv2298181
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTFDP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963365
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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