A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509869



Internal ID20883182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76965126..77435062hg38UCSC Ensembl
chr16:76999023..77468959hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38469937
hg19469937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186833
Samples
Known GenesADAMTS18, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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