A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378104



Internal ID21035657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32657492..32698790hg38UCSC Ensembl
chr5:32657598..32698896hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3841299
hg1941299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378104
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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