A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212212



Internal ID20779252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186688722..186778386hg38UCSC Ensembl
chr3:186406511..186496175hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3889665
hg1989665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361243
Supporting Variants
Samples
Known GenesKNG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212212
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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