A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365372



Internal ID21022925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4842079..4845497hg38UCSC Ensembl
chr4:4843806..4847224hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg383419
hg193419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365372
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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