A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670536



Internal ID9936641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61840228..61840600hg38UCSC Ensembl
Outerchr11:61840191..61840650hg38UCSC Ensembl
Innerchr11:61607700..61608072hg19UCSC Ensembl
Outerchr11:61607663..61608122hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6057832
SamplesNA19678
Known GenesFADS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670536
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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