A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097658



Internal ID20664698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185105647..185110930hg38UCSC Ensembl
chr3:184823435..184828718hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg385284
hg195284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371242
Supporting Variants
Samples
Known GenesC3orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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