A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664376



Internal ID9930481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19655439..19663917hg38UCSC Ensembl
chr11:19676985..19685463hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388479
hg198479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5425627, essv6366184, essv5521966
SamplesHG00635, HG00578, HG00581
Known GenesNAV2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664376
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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