A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367516



Internal ID21025069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183606001..183633190hg38UCSC Ensembl
chr3:183323789..183350978hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3827190
hg1927190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367516
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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