A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345484



Internal ID21003037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165952901..165956500hg38UCSC Ensembl
chr2:166809411..166813010hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207353
Samples
Known GenesTTC21B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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