A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007455



Internal ID20574495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26365401..26366700hg38UCSC Ensembl
chr13:26939538..26940837hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475668
Supporting Variants
Samples
Known GenesCDK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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