A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092047



Internal ID20659087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111109401..111110200hg38UCSC Ensembl
chr3:110828248..110829047hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372357
Supporting Variants
Samples
Known GenesPVRL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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