A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093990



Internal ID22003223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111221254..111221254hg38UCSC Ensembl
chr13:111873601..111873601hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600909
Samples
Known GenesARHGEF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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