A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626199



Internal ID6666348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47220929..47225361hg38UCSC Ensembl
Innerchr11:47220992..47225298hg38UCSC Ensembl
Outerchr11:47220866..47225424hg38UCSC Ensembl
chr11:47242480..47246912hg19UCSC Ensembl
Innerchr11:47242543..47246849hg19UCSC Ensembl
Outerchr11:47242417..47246975hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg384433
hg194433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14120108, essv14120110, essv14120109
SamplesHG03965, HG03862, NA19072
Known GenesDDB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626199
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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