A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671534



Internal ID9937639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11002330..11002576hg38UCSC Ensembl
chr11:11023877..11024123hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38247
hg19247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6181702, essv6459120, essv5501678, essv6555503, essv6337129
SamplesHG00249, HG01083, HG00277, HG01390, HG00125
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671534
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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