A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355677



Internal ID21013230
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 StatusM
Merged Variants
Supporting Variantsnssv18210510
Samples
Known GenesSTT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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