A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5454623



Internal ID8432026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28519923..28523621hg38UCSC Ensembl
chr17:26846941..26850639hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg383699
hg193699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667706
Supporting Variants
SamplesNA12347
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5454623
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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