A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093536



Internal ID22002769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94144047..94144047hg38UCSC Ensembl
chr13:94796301..94796301hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617248
Samples
Known GenesGPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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