A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478862



Internal ID21136415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61716007..61762889hg38UCSC Ensembl
chr13:62290140..62337022hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3846883
hg1946883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196961
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478862
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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