A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094965



Internal ID20662005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136849745..136852745hg38UCSC Ensembl
chr3:136568587..136571587hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg383001
hg193001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357282
Supporting Variants
Samples
Known GenesSLC35G2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094965
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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