A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094818



Internal ID20661858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:134218999..134219684hg38UCSC Ensembl
chr3:133937843..133938528hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372647
Supporting Variants
Samples
Known GenesRYK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094818
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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