A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627429



Internal ID7014258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97963349..97967260hg38UCSC Ensembl
Innerchr11:97963355..97967255hg38UCSC Ensembl
Outerchr11:97963344..97967266hg38UCSC Ensembl
chr11:97834077..97837988hg19UCSC Ensembl
Innerchr11:97834083..97837983hg19UCSC Ensembl
Outerchr11:97834072..97837994hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383912
hg193912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14246577, essv14246576, essv14246578, essv14246579, essv14246575
SamplesHG01326, HG00739, NA18945, HG01086, HG00595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627429
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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