A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625260



Internal ID7012095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6123720..6150612hg38UCSC Ensembl
Innerchr11:6123720..6150612hg38UCSC Ensembl
Outerchr11:6123220..6151112hg38UCSC Ensembl
chr11:6144950..6171842hg19UCSC Ensembl
Innerchr11:6144950..6171842hg19UCSC Ensembl
Outerchr11:6144450..6172342hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826893
hg1926893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14009008, essv14009007
SamplesHG01762, HG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625260
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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