A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501877



Internal ID20875115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14286497..14309905hg38UCSC Ensembl
chr16:14380354..14403762hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3823409
hg1923409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179143
Samples
Known GenesMIR193B, MIR365A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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