A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007691



Internal ID20574731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20881561..20884002hg38UCSC Ensembl
chr13:21455700..21458141hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg382442
hg192442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481426
Supporting Variants
Samples
Known GenesXPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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