A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14271046



Internal ID6380001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106253578..106254398hg38UCSC Ensembl
Innerchr11:106253587..106254390hg38UCSC Ensembl
Outerchr11:106253570..106254407hg38UCSC Ensembl
chr11:106124305..106125125hg19UCSC Ensembl
Innerchr11:106124314..106125117hg19UCSC Ensembl
Outerchr11:106124297..106125134hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627630
Supporting Variants
SamplesNA20320
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14271046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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