A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200692



Internal ID20767732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:246121868..246457377hg38UCSC Ensembl
chr1:246285170..246620679hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38335510
hg19335510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332874
Supporting Variants
Samples
Known GenesSMYD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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