A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18130295



Internal ID20697335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20053784..20136447hg38UCSC Ensembl
chr5:20053893..20136556hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3882664
hg1982664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380033
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18130295
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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