A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122836



Internal ID20689876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115067594..115069103hg38UCSC Ensembl
chr5:114403291..114404800hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg381510
hg191510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404600
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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