A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025438



Internal ID20592478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66899455..66904680hg38UCSC Ensembl
chr15:67191793..67197018hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385226
hg195226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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