A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483886



Internal ID21141439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92644056..93213914hg38UCSC Ensembl
chr13:93296309..93866167hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38569859
hg19569859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183161
Samples
Known GenesGPC5, GPC5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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