A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363051



Internal ID21020604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67651901..67657400hg38UCSC Ensembl
chr3:67702325..67707824hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213004
Samples
Known GenesSUCLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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