A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672600



Internal ID9938705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75521803..75522608hg38UCSC Ensembl
chr9:78136719..78137524hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5508615, essv6009626
SamplesHG01204, NA19779
Known GenesMIR548H3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672600
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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