A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201810



Internal ID20768851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20127045..20133948hg38UCSC Ensembl
chr1:20453538..20460441hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386904
hg196904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201810
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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