A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185500



Internal ID20752540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99083222..99114521hg38UCSC Ensembl
chr13:99735476..99766775hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3831300
hg1931300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481457
Supporting Variants
Samples
Known GenesDOCK9, DOCK9-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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