A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504460



Internal ID20877721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14894701..15045500hg38UCSC Ensembl
chr16:14988558..15139357hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38150800
hg19150800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193357
Samples
Known GenesLOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NTAN1, PDXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504460
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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