A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182387



Internal ID20749427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95238075..95295847hg38UCSC Ensembl
chr13:95890329..95948101hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3857773
hg1957773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6485917
Supporting Variants
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182387
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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