A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14071732



Internal ID4073548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:27146261..27150584hg38UCSC Ensembl
Innerchr11:27146266..27150580hg38UCSC Ensembl
Outerchr11:27146257..27150589hg38UCSC Ensembl
chr11:27167808..27172131hg19UCSC Ensembl
Innerchr11:27167813..27172127hg19UCSC Ensembl
Outerchr11:27167804..27172136hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg384324
hg194324
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625765
Supporting Variants
SamplesHG02642
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14071732
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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