A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14314598



Internal ID5883199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131240077..131246315hg38UCSC Ensembl
Innerchr11:131240077..131246315hg38UCSC Ensembl
Outerchr11:131239577..131246815hg38UCSC Ensembl
chr11:131109972..131116210hg19UCSC Ensembl
Innerchr11:131109972..131116210hg19UCSC Ensembl
Outerchr11:131109472..131116710hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg386239
hg196239
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628101
Supporting Variants
SamplesNA19309
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14314598
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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