A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682788



Internal ID15072754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22512740..22528966hg38UCSC Ensembl
Innerchr8:22370253..22386479hg19UCSC Ensembl
Innerchr8:22426198..22442424hg18UCSC Ensembl
Innerchr8:22426198..22442424hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3816227
hg1916227
hg1816227
hg1716227
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517680
Supporting Variants
Samples
Known GenesPPP3CC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682788
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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