A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18123805



Internal ID20690846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114542813..114549614hg38UCSC Ensembl
chr5:113878510..113885311hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg386802
hg196802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18123805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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