A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507284



Internal ID20880572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28217923..28240835hg38UCSC Ensembl
chr16:28229244..28252156hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3822913
hg1922913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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