A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211629



Internal ID20778669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67352729..67439106hg38UCSC Ensembl
chr4:68218447..68304824hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3886378
hg1986378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6388036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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