A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653455



Internal ID21601760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36142665..36142665hg38UCSC Ensembl
chr13:36716802..36716802hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096020
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653455
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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