A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489541



Internal ID21147094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74738799..74741056hg38UCSC Ensembl
chr13:75312936..75315193hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg382258
hg192258
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489541
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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