A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663701



Internal ID9583120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123548534..123550135hg38UCSC Ensembl
chr11:123419242..123420843hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6081419
SamplesHG00159
Known GenesGRAMD1B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663701
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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