A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1957n223



Internal ID22804925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:88861902..89040182hg38UCSC Ensembl
chr13:89514156..89692436hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38178281
hg19178281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6486638, nsv6494516
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1957n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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