A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14211155



Internal ID2381769
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626804
Supporting Variants
SamplesHG02111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14211155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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