A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086427



Internal ID21472916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111340476..111340476hg38UCSC Ensembl
chr13:111992823..111992823hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649406
Supporting Variants
SamplesHG03371
Known GenesTEX29
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086427
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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