A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211177



Internal ID20778217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36681629..36707006hg38UCSC Ensembl
chr3:36723120..36748497hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3825378
hg1925378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360796
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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