A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18136045



Internal ID20703085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86677779..86678439hg38UCSC Ensembl
chr5:85973596..85974256hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18136045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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