A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478928



Internal ID21136481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87977437..87992122hg38UCSC Ensembl
chr13:88629692..88644377hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3814686
hg1914686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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