A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212285



Internal ID20779325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57748201..57752000hg38UCSC Ensembl
chr3:57733928..57737727hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212285
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00087


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