A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6241302



Internal ID9448158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107363690..107373246hg38UCSC Ensembl
Outerchr11:107363269..107373666hg38UCSC Ensembl
Innerchr11:107234416..107243972hg19UCSC Ensembl
Outerchr11:107233995..107244392hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672284
Supporting Variants
SamplesNA18868
Known GenesCWF19L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6241302
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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