A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5381n223



Internal ID22808349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97761547..98260663hg38UCSC Ensembl
chr4:98682698..99181814hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38499117
hg19499117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6392674, nsv6387914
Samples
Known GenesSTPG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5381n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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