A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614440



Internal ID7001334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106287297..106304921hg38UCSC Ensembl
Innerchr7:106287447..106304771hg38UCSC Ensembl
Outerchr7:106287147..106305071hg38UCSC Ensembl
chr7:105927743..105945367hg19UCSC Ensembl
Innerchr7:105927893..105945217hg19UCSC Ensembl
Outerchr7:105927593..105945517hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3817625
hg1917625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1316e214
Supporting Variantsessv12917380, essv12917385, essv12917382, essv12917384, essv12917383, essv12917381
SamplesHG03738, NA19917, HG04035, HG03949, NA21090, HG01583
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614440
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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