A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967074



Internal ID18602303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139494060..139497820hg38UCSC Ensembl
Innerchr3:139212902..139216662hg19UCSC Ensembl
Innerchr3:140695592..140699352hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383761
hg193761
hg183761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2296989, nssv2296984, nssv2296986, nssv2296988, nssv2296991, nssv2296990, nssv2296987, nssv2296983, nssv2296992, nssv2296985
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)nsv967074
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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