A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505459



Internal ID20878729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29608327..29609794hg38UCSC Ensembl
chr16:29619648..29621115hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381468
hg191468
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186041
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505459
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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