A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627195



Internal ID6667343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90231206..90288834hg38UCSC Ensembl
chr11:89964374..90022002hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3857629
hg1957629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv220e214
Supporting Variantsessv14231036, essv14231035, essv14231037
SamplesHG02780, NA19756, HG02684
Known GenesDISC1FP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627195
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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