A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676702



Internal ID15066668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14650667..14659785hg38UCSC Ensembl
Innerchr8:14508176..14517294hg19UCSC Ensembl
Innerchr8:14552547..14561665hg18UCSC Ensembl
Innerchr8:14552547..14561665hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg389119
hg199119
hg189119
hg179119
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517019
Supporting Variants
Samples
Known GenesSGCZ
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676702
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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