A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210510



Internal ID20777550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31531801..31533500hg38UCSC Ensembl
chr3:31573293..31574992hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355677
Supporting Variants
Samples
Known GenesSTT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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