A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967108



Internal ID18602337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:196528603..196537099hg38UCSC Ensembl
Innerchr3:196255474..196263970hg19UCSC Ensembl
Innerchr3:197739871..197748367hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg388497
hg198497
hg188497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2310845, nssv2310839, nssv2310841, nssv2310842, nssv2310847, nssv2310843, nssv2310846, nssv2310844, nssv2310840, nssv2310838
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)nsv967108
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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