A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv519n209



Internal ID22826594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22933611..24388560hg38UCSC Ensembl
chr13:23507750..24962698hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381454950
hg191454949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5938299, nsv5928055, nsv5936669, nsv5927619, nsv5943116
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv519n209
Frequency
Sample Size914
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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