A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357062



Internal ID21014615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142100647..142368380hg38UCSC Ensembl
chr3:141819489..142087222hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38267734
hg19267734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209652
Samples
Known GenesGK5, TFDP2, XRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357062
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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