A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659903



Internal ID9926008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133252413..133258230hg38UCSC Ensembl
chr9:136127800..136133621hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg385818
hg195822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6180286, essv6331846, essv5988006, essv6433667, essv5589617
SamplesNA18520, NA19982, NA19375, NA18909, NA19102
Known GenesABO
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659903
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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