A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092074



Internal ID22001307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35436160..35436160hg38UCSC Ensembl
chr13:36010297..36010297hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605070
Samples
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092074
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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