A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092117



Internal ID20659157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112109117..112118509hg38UCSC Ensembl
chr3:111827964..111837356hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg389393
hg199393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373671
Supporting Variants
Samples
Known GenesC3orf52, MIR567
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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