A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345875



Internal ID21003428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12105..55657hg38UCSC Ensembl
chr3:60001..97340hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3843553
hg1937340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345875
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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