A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015349



Internal ID20582389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94455197..94457291hg38UCSC Ensembl
chr13:95107451..95109545hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg382095
hg192095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477489
Supporting Variants
Samples
Known GenesDCT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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