A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367780



Internal ID21025333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39956670..39957406hg38UCSC Ensembl
chr3:39998161..39998897hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100916
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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