A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026867



Internal ID20593907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80580692..80581057hg38UCSC Ensembl
chr15:80873033..80873398hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511832
Supporting Variants
Samples
Known GenesARNT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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