A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492902



Internal ID21150455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108216101..108222200hg38UCSC Ensembl
chr13:108868449..108874548hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187590
Samples
Known GenesABHD13, LIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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