A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026575



Internal ID20593615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72274691..72280022hg38UCSC Ensembl
chr15:72567032..72572363hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385332
hg195332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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