A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626804



Internal ID7013634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72549215..72550535hg38UCSC Ensembl
Innerchr11:72549215..72550535hg38UCSC Ensembl
Outerchr11:72548904..72550730hg38UCSC Ensembl
chr11:72260259..72261579hg19UCSC Ensembl
Innerchr11:72260259..72261579hg19UCSC Ensembl
Outerchr11:72259948..72261774hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14211155, essv14211156, essv14211154, essv14211157
SamplesHG02111, HG02073, NA20342, HG02307
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626804
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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