A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614441



Internal ID7001335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106289240..106304906hg38UCSC Ensembl
chr7:105929686..105945352hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3815667
hg1915667
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1316e214
Supporting Variantsessv12917388, essv12917389, essv12917387, essv12917390, essv12917386
SamplesHG03738, HG04035, HG03949, NA21090, HG01583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614441
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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