A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657357



Internal ID9923462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124811884..124812870hg38UCSC Ensembl
chr11:124681780..124682766hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6350714, essv6458559, essv6567567, essv6164495
SamplesNA19372, NA18907, NA20276, HG01191
Known GenesLOC100507283
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657357
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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