A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102142



Internal ID20669182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3736550..3831236hg38UCSC Ensembl
chr3:3778234..3872920hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3894687
hg1994687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362595
Supporting Variants
Samples
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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