A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026857



Internal ID20593897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80286812..80289700hg38UCSC Ensembl
chr15:80579154..80582042hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382889
hg192889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501192
Supporting Variants
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026857
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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