A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487419



Internal ID21144972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19002416..19008342hg38UCSC Ensembl
chr13:19576556..19582482hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg385927
hg195927
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187778
Samples
Known GenesLINC00442
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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