A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478479



Internal ID21136032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27165511..27199787hg38UCSC Ensembl
chr13:27739648..27773924hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3834277
hg1934277
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194382
Samples
Known GenesUSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478479
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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