A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596001



Internal ID21544608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111591756..111591872hg38UCSC Ensembl
chr13:112244103..112244219hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099206
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596001
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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