A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590169



Internal ID21538738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42181816..42182067hg38UCSC Ensembl
chr13:42755952..42756203hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081651
SamplesHG00731
Known GenesDGKH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590169
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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