A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360911



Internal ID21018464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4222496..4230608hg38UCSC Ensembl
chr3:4264180..4272292hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg388113
hg198113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099891
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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