A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211195



Internal ID20778235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3836896..3840109hg38UCSC Ensembl
chr3:3878580..3881793hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg383214
hg193214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360107
Supporting Variants
Samples
Known GenesLRRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211195
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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