A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488529



Internal ID21146082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65065311..65112691hg38UCSC Ensembl
chr13:65639443..65686823hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3847381
hg1947381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195844
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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