A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023942



Internal ID20590982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42496513..42498466hg38UCSC Ensembl
chr15:42788711..42790664hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381954
hg191954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505534
Supporting Variants
Samples
Known GenesSNAP23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023942
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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