A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026873



Internal ID20593913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89206897..89214258hg38UCSC Ensembl
chr15:89750128..89757489hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387362
hg197362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513719
Supporting Variants
Samples
Known GenesRLBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026873
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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