A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6328629



Internal ID9758199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100923496..100925551hg38UCSC Ensembl
Outerchr11:100923444..100925602hg38UCSC Ensembl
Innerchr11:100794227..100796282hg19UCSC Ensembl
Outerchr11:100794175..100796333hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659208
Supporting Variants
SamplesNA19712
Known GenesARHGAP42
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6328629
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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