A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597615



Internal ID21546231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111688072..111688173hg38UCSC Ensembl
chr13:112340419..112340520hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091921
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597615
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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