A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511627



Internal ID20884957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:187359..200216hg38UCSC Ensembl
chr16:237358..250215hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812858
hg1912858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177268
Samples
Known GenesLUC7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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