A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024516



Internal ID20591556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40304237..40310972hg38UCSC Ensembl
chr15:40596438..40603173hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386736
hg196736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504007
Supporting Variants
Samples
Known GenesPLCB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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