A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024479



Internal ID21933822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111125466..111125780hg38UCSC Ensembl
chr13:111777813..111778127hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601335
Samples
Known GenesARHGEF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024479
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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