A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696285



Internal ID15086251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:169659667..169705401hg38UCSC Ensembl
Innerchr4:170580818..170626552hg19UCSC Ensembl
Innerchr4:170817393..170863127hg18UCSC Ensembl
Innerchr4:170955548..171001282hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3845735
hg1945735
hg1845735
hg1745735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518832
Supporting Variants
Samples
Known GenesCLCN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696285
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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