A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026737



Internal ID20593777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85814101..85822300hg38UCSC Ensembl
chr15:86357332..86365531hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00181


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