A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392247



Internal ID21049800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54218401..54224100hg38UCSC Ensembl
chr4:55084568..55090267hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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