A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662808



Internal ID9928913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60803991..60804657hg38UCSC Ensembl
Outerchr11:60803954..60804707hg38UCSC Ensembl
Innerchr11:60571464..60572130hg19UCSC Ensembl
Outerchr11:60571427..60572180hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6579678
SamplesNA19780
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662808
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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