A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088472



Internal ID21502228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32258752..32258752hg38UCSC Ensembl
chr13:32832889..32832889hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5645715
Supporting Variants
SamplesNA19239
Known GenesFRY
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088472
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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