A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104239



Internal ID20671279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8835606..8836304hg38UCSC Ensembl
chr3:8877290..8877988hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38699
hg19699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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