A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203938



Internal ID20770978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36103929..36247487hg38UCSC Ensembl
chr21:37476227..37619785hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38143559
hg19143559
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537307
Supporting Variants
Samples
Known GenesCBR3, CBR3-AS1, DOPEY2, LOC100133286
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203938
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00155


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