A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18135189



Internal ID20702229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83817650..83818301hg38UCSC Ensembl
chr5:83113469..83114120hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18135189
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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