A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181536



Internal ID20748576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87034861..87046906hg38UCSC Ensembl
chr15:87578092..87590137hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3812046
hg1912046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181536
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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