A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102672



Internal ID20669712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49537718..49538312hg38UCSC Ensembl
chr3:49575151..49575745hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00017


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