A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6237966



Internal ID9215369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6409642..6409837hg38UCSC Ensembl
chr11:6430872..6431067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667097
Supporting Variants
SamplesNA18499
Known GenesAPBB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6237966
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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