A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14071737



Internal ID4073553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27328141..27335102hg38UCSC Ensembl
Innerchr11:27328141..27335102hg38UCSC Ensembl
Outerchr11:27327641..27335602hg38UCSC Ensembl
chr11:27349688..27356649hg19UCSC Ensembl
Innerchr11:27349688..27356649hg19UCSC Ensembl
Outerchr11:27349188..27357149hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386962
hg196962
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625768
Supporting Variants
SamplesHG03653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14071737
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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