A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14100668



Internal ID3396306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39583826..39604154hg38UCSC Ensembl
Innerchr11:39583826..39604154hg38UCSC Ensembl
Outerchr11:39583591..39604225hg38UCSC Ensembl
chr11:39605376..39625704hg19UCSC Ensembl
Innerchr11:39605376..39625704hg19UCSC Ensembl
Outerchr11:39605141..39625775hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3820329
hg1920329
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626044
Supporting Variants
SamplesHG03046
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14100668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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