A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134274



Internal ID20701314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89886414..89886865hg38UCSC Ensembl
chr5:89182231..89182682hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414023
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00064


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