A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14210463



Internal ID3892611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71501694..71504680hg38UCSC Ensembl
Innerchr11:71501695..71504679hg38UCSC Ensembl
Outerchr11:71501693..71504681hg38UCSC Ensembl
chr11:71212740..71215726hg19UCSC Ensembl
Innerchr11:71212741..71215725hg19UCSC Ensembl
Outerchr11:71212739..71215727hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626777
Supporting Variants
SamplesHG03547
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14210463
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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