A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595490



Internal ID21544096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108239546..108256058hg38UCSC Ensembl
chr13:108891894..108908406hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3816513
hg1916513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085848
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595490
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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