A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487797



Internal ID21145350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92305352..92397194hg38UCSC Ensembl
chr13:92957605..93049447hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3891843
hg1991843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194557
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487797
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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