A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511617



Internal ID20884947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9112648..9230502hg38UCSC Ensembl
chr16:9206505..9324359hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38117855
hg19117855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182778
Samples
Known GenesC16orf72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511617
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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