A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628062



Internal ID7014887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129318628..129349115hg38UCSC Ensembl
Innerchr11:129318628..129349115hg38UCSC Ensembl
Outerchr11:129318128..129349615hg38UCSC Ensembl
chr11:129188523..129219010hg19UCSC Ensembl
Innerchr11:129188523..129219010hg19UCSC Ensembl
Outerchr11:129188023..129219510hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3830488
hg1930488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14310156
SamplesHG02660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628062
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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