A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086322



Internal ID21452526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113600651..113600740hg38UCSC Ensembl
chr13:114254966..114255055hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594955
Supporting Variants
SamplesHG01596
Known GenesTFDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086322
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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