A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486843



Internal ID21144396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91398301..91400000hg38UCSC Ensembl
chr13:92050555..92052254hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182560
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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