A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512012



Internal ID20885342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36081819..36188203hg38UCSC Ensembl
chr17:34409176..34515579hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106385
hg19106404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3094n223
Supporting Variantsnssv18182505
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer