A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103195



Internal ID20670235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84084298..84095487hg38UCSC Ensembl
chr3:84133449..84144638hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3811190
hg1911190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368873
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00059


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