A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187603



Internal ID20754643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24209670..24516475hg38UCSC Ensembl
chr15:24454817..24761622hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38306806
hg19306806
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501317
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187603
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0003


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