A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105425



Internal ID20672465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94944178..95025090hg38UCSC Ensembl
chr3:94663022..94743934hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3880913
hg1980913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363915
Supporting Variants
Samples
Known GenesLINC00879
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105425
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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