A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212150



Internal ID20779190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183452695..183463418hg38UCSC Ensembl
chr3:183170483..183181206hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3810724
hg1910724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357594
Supporting Variants
Samples
Known GenesLINC00888
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212150
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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