A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009287



Internal ID20576329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:54212011..54247991hg38UCSC Ensembl
chr13:54786146..54822126hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3835981
hg1935981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478572
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0011


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