A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14223416



Internal ID416818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86820694..86823905hg38UCSC Ensembl
Innerchr11:86820702..86823898hg38UCSC Ensembl
Outerchr11:86820687..86823913hg38UCSC Ensembl
chr11:86531736..86534947hg19UCSC Ensembl
Innerchr11:86531744..86534940hg19UCSC Ensembl
Outerchr11:86531729..86534955hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383212
hg193212
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627105
Supporting Variants
SamplesHG00126
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14223416
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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