A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6081419



Internal ID9058822
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 StatusS
Merged Variantsesv2663701
Supporting Variants
SamplesHG00159
Known GenesGRAMD1B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6081419
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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