A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627377



Internal ID7014206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96281150..96293837hg38UCSC Ensembl
Innerchr11:96281191..96293797hg38UCSC Ensembl
Outerchr11:96281110..96293878hg38UCSC Ensembl
chr11:96014314..96027001hg19UCSC Ensembl
Innerchr11:96014355..96026961hg19UCSC Ensembl
Outerchr11:96014274..96027042hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3812688
hg1912688
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245165
SamplesHG02461
Known GenesMAML2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627377
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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