A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499058



Internal ID20872274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30796270..30800569hg38UCSC Ensembl
chr16:30807591..30811890hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180206
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499058
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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