A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477455



Internal ID21135008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91128487..91151266hg38UCSC Ensembl
chr13:91780741..91803520hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3822780
hg1922780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191963
Samples
Known GenesLINC00379
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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