A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628061



Internal ID7014886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129236310..129240259hg38UCSC Ensembl
Innerchr11:129236312..129240257hg38UCSC Ensembl
Outerchr11:129236308..129240261hg38UCSC Ensembl
chr11:129106205..129110154hg19UCSC Ensembl
Innerchr11:129106207..129110152hg19UCSC Ensembl
Outerchr11:129106203..129110156hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg383950
hg193950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14310155, essv14310154
SamplesHG01971, HG02312
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628061
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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