A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212393



Internal ID20779433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77817901..77820500hg38UCSC Ensembl
chr4:78739055..78741654hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383345
Supporting Variants
Samples
Known GenesCNOT6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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