A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6030756



Internal ID9008159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118547983..118548600hg38UCSC Ensembl
chr11:118418698..118419315hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666357
Supporting Variants
SamplesNA19468
Known GenesIFT46
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6030756
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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