A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502607



Internal ID20875853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18784377..18799306hg38UCSC Ensembl
chr16:18795699..18810628hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3814930
hg1914930
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189046
Samples
Known GenesARL6IP1, RPS15A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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