A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096716



Internal ID22005949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113148345..113148345hg38UCSC Ensembl
chr13:113802659..113802659hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614215
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096716
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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