A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652920



Internal ID21601225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26559809..26559809hg38UCSC Ensembl
chr13:27133946..27133946hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096418
SamplesHG00096
Known GenesWASF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652920
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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