A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027319



Internal ID20594359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92842193..92854472hg38UCSC Ensembl
chr15:93385423..93397702hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812280
hg1912280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512954
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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