A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1953n223



Internal ID22804921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87640101..87705000hg38UCSC Ensembl
chr13:88292356..88357255hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3864900
hg1964900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6476340, nsv6478135, nsv6484471
Samples
Known GenesMIR4500HG, SLITRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1953n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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