A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv971659



Internal ID18606876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:65377393..65379458hg38UCSC Ensembl
Innerchr8:66289628..66291693hg19UCSC Ensembl
Innerchr8:66452182..66454247hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2506407, nssv2506404, nssv2506410, nssv2506402, nssv2506409, nssv2506406, nssv2506405, nssv2506401, nssv2506408, nssv2506403
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)nsv971659
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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