A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491056



Internal ID21148609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99641482..99650054hg38UCSC Ensembl
chr13:100293736..100302308hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg388573
hg198573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016425
Samples
Known GenesCLYBL, MIR4306
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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