A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626128



Internal ID7012962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42810119..42813600hg38UCSC Ensembl
Innerchr11:42810121..42813598hg38UCSC Ensembl
Outerchr11:42810117..42813602hg38UCSC Ensembl
chr11:42831669..42835150hg19UCSC Ensembl
Innerchr11:42831671..42835148hg19UCSC Ensembl
Outerchr11:42831667..42835152hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg383482
hg193482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14111581, essv14111580
SamplesHG02574, HG02573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626128
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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