A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093242



Internal ID22002475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46619064..46619064hg38UCSC Ensembl
chr13:47193199..47193199hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605380
Samples
Known GenesLRCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093242
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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