A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520882



Internal ID15101489
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683297, nssv676886
Samples
Known GenesLZTS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520882
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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