A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626201



Internal ID6666350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47343873..47345065hg38UCSC Ensembl
Innerchr11:47343873..47345065hg38UCSC Ensembl
Outerchr11:47343793..47345138hg38UCSC Ensembl
chr11:47365424..47366616hg19UCSC Ensembl
Innerchr11:47365424..47366616hg19UCSC Ensembl
Outerchr11:47365344..47366689hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14120113
SamplesNA19681
Known GenesMYBPC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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