A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614352



Internal ID6654558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102441080..102443935hg38UCSC Ensembl
Innerchr7:102441130..102443885hg38UCSC Ensembl
Outerchr7:102441030..102443985hg38UCSC Ensembl
chr7:102081527..102084382hg19UCSC Ensembl
Innerchr7:102081577..102084332hg19UCSC Ensembl
Outerchr7:102081477..102084432hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12911603
SamplesNA19901
Known GenesORAI2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614352
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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