A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv217n172



Internal ID22814591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110906897..110907305hg38UCSC Ensembl
chr13:111559244..111559652hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4431900, nsv4431901
SamplesBTQ016, NB07
Known GenesANKRD10
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv217n172
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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