A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5767531



Internal ID9397272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35561800..35562104hg38UCSC Ensembl
chr17:33888819..33889123hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663947
Supporting Variants
SamplesNA18602
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5767531
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