A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652070



Internal ID21600375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26559788..26559788hg38UCSC Ensembl
chr13:27133925..27133925hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091190
SamplesHG01114
Known GenesWASF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652070
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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