A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6554081



Internal ID9531484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:883923..889918hg38UCSC Ensembl
Outerchr11:883886..889968hg38UCSC Ensembl
Innerchr11:883923..889918hg19UCSC Ensembl
Outerchr11:883886..889968hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg386083
hg196083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671662
Supporting Variants
SamplesHG00242
Known GenesCHID1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6554081
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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