A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672745



Internal ID9938850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44708256..44711973hg38UCSC Ensembl
Outerchr11:44708099..44712126hg38UCSC Ensembl
Innerchr11:44729806..44733523hg19UCSC Ensembl
Outerchr11:44729649..44733676hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384028
hg194028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5724529, essv6298546, essv6297076, essv5732679
SamplesHG00442, HG00427, HG00418, NA18577
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672745
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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