A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971662



Internal ID18606879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67580776..67582657hg38UCSC Ensembl
Innerchr8:68493011..68494892hg19UCSC Ensembl
Innerchr8:68655565..68657446hg18UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381882
hg191882
hg181882
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2508066, nssv2508063, nssv2508062, nssv2508059, nssv2508064, nssv2508065, nssv2508061, nssv2508060, nssv2508058, nssv2508067
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCPA6
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv971662
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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