A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628111



Internal ID6668255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131751859..131777274hg38UCSC Ensembl
Innerchr11:131751859..131777274hg38UCSC Ensembl
Outerchr11:131751359..131777774hg38UCSC Ensembl
chr11:131621753..131647168hg19UCSC Ensembl
Innerchr11:131621753..131647168hg19UCSC Ensembl
Outerchr11:131621253..131647668hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3825416
hg1925416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317092
SamplesHG01437
Known GenesNTM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628111
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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