A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625161



Internal ID7011998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3957072..3995291hg38UCSC Ensembl
Innerchr11:3957072..3995291hg38UCSC Ensembl
Outerchr11:3956572..3995791hg38UCSC Ensembl
chr11:3978302..4016521hg19UCSC Ensembl
Innerchr11:3978302..4016521hg19UCSC Ensembl
Outerchr11:3977802..4017021hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3838220
hg1938220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13997093
SamplesHG02805
Known GenesSTIM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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