A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212988



Internal ID20780028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6646662..6783181hg38UCSC Ensembl
chr3:6688349..6824868hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38136520
hg19136520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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