A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023709



Internal ID20590749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26968283..26968609hg38UCSC Ensembl
chr15:27213430..27213756hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01539


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