A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086538



Internal ID21434387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113625285..113625285hg38UCSC Ensembl
chr13:114279600..114279600hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649515
Supporting Variants
SamplesHG00731
Known GenesTFDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086538
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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