A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627772



Internal ID6667919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113055966..113077647hg38UCSC Ensembl
Innerchr11:113055972..113077641hg38UCSC Ensembl
Outerchr11:113055960..113077653hg38UCSC Ensembl
chr11:112926688..112948369hg19UCSC Ensembl
Innerchr11:112926694..112948363hg19UCSC Ensembl
Outerchr11:112926682..112948375hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3821682
hg1921682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14287964, essv14287965
SamplesNA21106, NA20869
Known GenesNCAM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627772
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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