A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098263



Internal ID20665303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185872158..185875723hg38UCSC Ensembl
chr3:185589946..185593511hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383566
hg193566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370279
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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