A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5262n223



Internal ID22808230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47515112..47516025hg38UCSC Ensembl
chr4:47517129..47518042hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6564312, nsv6568139, nsv6570824
Samples
Known GenesATP10D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5262n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer