A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2433665



Internal ID17494068
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 StatusS
Merged Variantsnsv981428
Supporting Variants
SamplesHGDP00998
Known GenesCCZ1, OCM
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2433665
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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