A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356378



Internal ID21013931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27628101..27635400hg38UCSC Ensembl
chr3:27669592..27676891hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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