A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505904



Internal ID20879178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48417004..48530450hg38UCSC Ensembl
chr16:48450915..48564361hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38113447
hg19113447
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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