A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5934845



Internal ID8912248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63519672..63520884hg38UCSC Ensembl
Outerchr11:63519635..63520934hg38UCSC Ensembl
Innerchr11:63287144..63288356hg19UCSC Ensembl
Outerchr11:63287107..63288406hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669571
Supporting Variants
SamplesNA19383
Known GenesMIR3680-1, MIR3680-2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5934845
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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