A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023253



Internal ID20590294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26076898..26077816hg38UCSC Ensembl
chr15:26322045..26322963hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504376
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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