A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094874



Internal ID22004107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97147216..97147216hg38UCSC Ensembl
chr13:97799470..97799470hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg383007
hg193007
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094874
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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