A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497727



Internal ID20870935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14797501..14952600hg38UCSC Ensembl
chr16:14891358..15046457hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38155100
hg19155100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181678
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497727
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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