A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482813



Internal ID21140366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34553901..34555800hg38UCSC Ensembl
chr13:35128038..35129937hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179659
Samples
Known GenesLINC00457
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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