A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981428



Internal ID18269939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5860251..5915326hg38UCSC Ensembl
Innerchr7:5899882..5954957hg19UCSC Ensembl
Innerchr7:5866408..5921483hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3855076
hg1955076
hg1855076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2433663, nssv2433662, nssv2433665, nssv2433669, nssv2433664, nssv2433671, nssv2433668, nssv2433667, nssv2433670, nssv2433666
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCCZ1, OCM
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981428
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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