A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027329



Internal ID20594369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92882101..92883400hg38UCSC Ensembl
chr15:93425331..93426630hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512942
Supporting Variants
Samples
Known GenesLOC100507217
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07873


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