A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166011



Internal ID20733051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20697627..20698222hg38UCSC Ensembl
chr8:20555138..20555733hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426900
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166011
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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