A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627028



Internal ID7013858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83846373..83890278hg38UCSC Ensembl
chr11:83557416..83601321hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3843906
hg1943906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv214e214
Supporting Variantsessv14219953, essv14219952
SamplesNA18536, HG01846
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627028
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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