A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627392



Internal ID7014221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96976602..97009488hg38UCSC Ensembl
chr11:96847602..96880488hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3832887
hg1932887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14245418
SamplesHG02952
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627392
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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