A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6444258



Internal ID9219761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31372226..31376099hg38UCSC Ensembl
chr11:31393773..31397646hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383874
hg193874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660928
Supporting Variants
SamplesNA10851
Known GenesDNAJC24
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6444258
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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