A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094309



Internal ID21492225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113617547..113617610hg38UCSC Ensembl
chr13:114271862..114271925hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599483
Supporting Variants
SamplesNA19238
Known GenesTFDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094309
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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