A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496082



Internal ID20869280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31221188..31221940hg38UCSC Ensembl
chr16:31232509..31233261hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184093
Samples
Known GenesTRIM72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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