A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv563e199



Internal ID22758336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70106453..70108294hg38UCSC Ensembl
chr17:68102594..68104435hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381842
hg191842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2676947, esv2673868
SamplesNA19058, NA18592, NA18599, NA18612
Known GenesKCNJ16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv563e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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