A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663555



Internal ID9929660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123308609..123310084hg38UCSC Ensembl
chr9:126070888..126072363hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5446231, essv5687724, essv6358116
SamplesNA20769, HG01357, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663555
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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