A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588481



Internal ID21537044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86323257..86324360hg38UCSC Ensembl
chr13:86975512..86976615hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081123
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588481
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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