A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625781



Internal ID7012615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28179965..28208538hg38UCSC Ensembl
Innerchr11:28180015..28208488hg38UCSC Ensembl
Outerchr11:28179915..28208588hg38UCSC Ensembl
chr11:28201512..28230085hg19UCSC Ensembl
Innerchr11:28201562..28230035hg19UCSC Ensembl
Outerchr11:28201462..28230135hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3828574
hg1928574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14073372
SamplesHG03556
Known GenesMETTL15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625781
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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