A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485253



Internal ID21142806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86803287..88366930hg38UCSC Ensembl
chr13:87455542..89019185hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381563644
hg191563644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014047
Samples
Known GenesLINC00397, MIR4500, MIR4500HG, SLITRK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485253
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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