A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676886



Internal ID15066852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20244495..20251981hg38UCSC Ensembl
Innerchr8:20102006..20109492hg19UCSC Ensembl
Innerchr8:20146286..20153772hg18UCSC Ensembl
Innerchr8:20146286..20153772hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg387487
hg197487
hg187487
hg177487
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520882
Supporting Variants
Samples
Known GenesLZTS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676886
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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