A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494086



Internal ID21151639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20208301..20555300hg38UCSC Ensembl
chr13:20782440..21129439hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38347000
hg19347000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180235
Samples
Known GenesCRYL1, GJB6, MIR4499
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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