A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008456



Internal ID20575496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37598930..37599624hg38UCSC Ensembl
chr13:38173067..38173761hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490898
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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