A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014359



Internal ID20581399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89772916..90234328hg38UCSC Ensembl
chr13:90425170..90886582hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38461413
hg19461413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476950
Supporting Variants
Samples
Known GenesLINC00559, MIR622
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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