A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212219



Internal ID20779259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186860005..186997123hg38UCSC Ensembl
chr3:186577794..186714911hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38137119
hg19137118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370476
Supporting Variants
Samples
Known GenesST6GAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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