A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028622



Internal ID20595662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:97475365..97475957hg38UCSC Ensembl
chr15:98018595..98019187hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38593
hg19593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292


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