A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14211128



Internal ID1708192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72436936..72450486hg38UCSC Ensembl
Innerchr11:72436969..72450454hg38UCSC Ensembl
Outerchr11:72436904..72450519hg38UCSC Ensembl
chr11:72147980..72161530hg19UCSC Ensembl
Innerchr11:72148013..72161498hg19UCSC Ensembl
Outerchr11:72147948..72161563hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813551
hg1913551
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626800
Supporting Variants
SamplesHG01589
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14211128
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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