A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082501



Internal ID21488300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43995318..43995746hg38UCSC Ensembl
chr13:44569454..44569882hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586233
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082501
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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