A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14040157



Internal ID4656350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17382108..17384528hg38UCSC Ensembl
Innerchr11:17382125..17384511hg38UCSC Ensembl
Outerchr11:17382091..17384545hg38UCSC Ensembl
chr11:17403655..17406075hg19UCSC Ensembl
Innerchr11:17403672..17406058hg19UCSC Ensembl
Outerchr11:17403638..17406092hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382421
hg192421
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625476
Supporting Variants
SamplesHG04185
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14040157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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