A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499525



Internal ID20872746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37503375..37507762hg38UCSC Ensembl
chr17:35863481..35867868hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384388
hg194388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196722
Samples
Known GenesDUSP14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499525
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