A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008385



Internal ID20575425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36737801..36783300hg38UCSC Ensembl
chr13:37311938..37357437hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3845500
hg1945500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008385
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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