A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500831



Internal ID20874060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10669159..11475479hg38UCSC Ensembl
chr16:10763016..11569335hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38806321
hg19806320
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177784
Samples
Known GenesCIITA, CLEC16A, DEXI, NUBP1, PRM1, PRM2, PRM3, RMI2, SOCS1, TEKT5, TNP2, TVP23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500831
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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