A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675610



Internal ID9595029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131849801..131854667hg38UCSC Ensembl
chr11:131719695..131724561hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg384867
hg194867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5971431, essv6071943
SamplesHG00701, NA18562
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675610
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