A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18023211



Internal ID20590252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100912876..100913171hg38UCSC Ensembl
chr15:101453081..101453376hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510922
Supporting Variants
Samples
Known GenesALDH1A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18023211
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.54125


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