A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5356n223



Internal ID22808324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89910122..90031783hg38UCSC Ensembl
chr4:90831273..90952934hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38121662
hg19121662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6386026, nsv6379397
Samples
Known GenesMMRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5356n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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