A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966821



Internal ID18602051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65074517..65081191hg38UCSC Ensembl
Innerchr7:64534895..64541569hg19UCSC Ensembl
Innerchr7:64172330..64179004hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg386675
hg196675
hg186675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2455574, nssv2455575, nssv2455577, nssv2455578, nssv2455579, nssv2455582, nssv2455576, nssv2455573, nssv2455581, nssv2455580
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCT6P3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966821
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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