A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480123



Internal ID21137676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91348201..91352900hg38UCSC Ensembl
chr13:92000455..92005154hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194891
Samples
Known GenesMIR17, MIR17HG, MIR18A, MIR19A, MIR19B1, MIR20A, MIR92A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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