A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv136n206



Internal ID22755440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90874180..91063591hg38UCSC Ensembl
chr13:91526434..91715845hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38189412
hg19189412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5513375, nsv5505707
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv136n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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