A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981430



Internal ID18616627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6809440..6853466hg38UCSC Ensembl
Innerchr7:6849071..6893097hg19UCSC Ensembl
Innerchr7:6815596..6859622hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3844027
hg1944027
hg1844027
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2435407, nssv2435406, nssv2435404, nssv2435401, nssv2435403, nssv2435409, nssv2435405, nssv2435400, nssv2435408, nssv2435402
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCCZ1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981430
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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