A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495287



Internal ID21152840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51170135..51174862hg38UCSC Ensembl
chr13:51744271..51748998hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384728
hg194728
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185052
Samples
Known GenesLINC00371
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495287
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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