A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102162



Internal ID20669202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3775752..3843909hg38UCSC Ensembl
chr3:3817436..3885593hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3868158
hg1968158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366418
Supporting Variants
Samples
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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