A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656589



Internal ID9576008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94177637..94178077hg38UCSC Ensembl
chr11:93910803..93911243hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5508428, essv5910559, essv5706449, essv6582412, essv6327247, essv6232058, essv5918092, essv5839866, essv5945606, essv6323481, essv6230664, essv5796382, essv6033488, essv6544350, essv6572292, essv5672557, essv5842651, essv6245494
SamplesNA12249, NA07347, NA18520, HG00731, NA20531, NA18953, HG01204, NA20521, NA12763, NA12155, NA20754, NA12006, HG00263, NA12045, NA11829, NA18853, HG00136, HG00312
Known GenesPANX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656589
Frequency
Sample Size1151
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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