A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv967601



Internal ID18602829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:69943282..69946133hg38UCSC Ensembl
Innerchr8:70855517..70858368hg19UCSC Ensembl
Innerchr8:71018071..71020922hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382852
hg192852
hg182852
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2507505, nssv2507501, nssv2507500, nssv2507499, nssv2507504, nssv2507506, nssv2507503, nssv2507498, nssv2507497, nssv2507502
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)nsv967601
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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