A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095815



Internal ID21446830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18928139..18928955hg38UCSC Ensembl
chr13:19502279..19503095hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596527
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095815
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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