A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627998



Internal ID6668142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125964404..125965732hg38UCSC Ensembl
Innerchr11:125964433..125965703hg38UCSC Ensembl
Outerchr11:125964375..125965761hg38UCSC Ensembl
chr11:125834299..125835627hg19UCSC Ensembl
Innerchr11:125834328..125835598hg19UCSC Ensembl
Outerchr11:125834270..125835656hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302920
SamplesHG03999
Known GenesCDON
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627998
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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