A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093115



Internal ID20660155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112935043..112940395hg38UCSC Ensembl
chr3:112653890..112659242hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg385353
hg195353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366511
Supporting Variants
Samples
Known GenesCD200R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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