A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646402



Internal ID21594707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73610459..73610459hg38UCSC Ensembl
chr13:74184596..74184596hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099222
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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