A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080798



Internal ID21446480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71553080..71553129hg38UCSC Ensembl
chr13:72127212..72127261hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588105
Supporting Variants
SamplesHG00732
Known GenesDACH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080798
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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