A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026135



Internal ID20593175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58005766..58006346hg38UCSC Ensembl
chr15:58297964..58298544hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513472
Supporting Variants
Samples
Known GenesALDH1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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