A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212454



Internal ID20779494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114915201..114944000hg38UCSC Ensembl
chr5:114250898..114279697hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3828800
hg1928800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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