A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14236422



Internal ID6237271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93201602..93205578hg38UCSC Ensembl
Innerchr11:93201602..93205578hg38UCSC Ensembl
Outerchr11:93201387..93205834hg38UCSC Ensembl
chr11:92934768..92938744hg19UCSC Ensembl
Innerchr11:92934768..92938744hg19UCSC Ensembl
Outerchr11:92934553..92939000hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383977
hg193977
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627284
Supporting Variants
SamplesNA19762
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14236422
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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