A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181563



Internal ID20748603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57350452..57488224hg38UCSC Ensembl
chr15:57642650..57780422hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38137773
hg19137773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512003
Supporting Variants
Samples
Known GenesCGNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181563
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00112


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