A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489771



Internal ID21147324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21981676..22000254hg38UCSC Ensembl
chr13:22555815..22574393hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3818579
hg1918579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489771
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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