A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015131



Internal ID20582171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89290101..89292100hg38UCSC Ensembl
chr13:89942355..89944354hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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