A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13993512



Internal ID6028239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1806902..1811707hg38UCSC Ensembl
Innerchr11:1807402..1811207hg38UCSC Ensembl
Outerchr11:1805902..1812707hg38UCSC Ensembl
chr11:1828132..1832937hg19UCSC Ensembl
Innerchr11:1828632..1832437hg19UCSC Ensembl
Outerchr11:1827132..1833937hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384806
hg194806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625117
Supporting Variants
SamplesNA19436
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13993512
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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