A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212835



Internal ID20779875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18628801..18634500hg38UCSC Ensembl
chr4:18630424..18636123hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6356666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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