A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089998



Internal ID21501903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33558675..33564768hg38UCSC Ensembl
chr13:34132812..34138905hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg386094
hg196094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600837
Supporting Variants
SamplesNA19239
Known GenesSTARD13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089998
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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