A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209200



Internal ID20776240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169836012..169846987hg38UCSC Ensembl
chr3:169553800..169564775hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3810976
hg1910976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365848
Supporting Variants
Samples
Known GenesLRRC31, LRRIQ4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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