A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187778



Internal ID20754818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19002416..19008342hg38UCSC Ensembl
chr13:19576556..19582482hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg385927
hg195927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487419
Supporting Variants
Samples
Known GenesLINC00442
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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