A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614365



Internal ID7001259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102915265..102916359hg38UCSC Ensembl
Innerchr7:102915290..102916334hg38UCSC Ensembl
Outerchr7:102915240..102916384hg38UCSC Ensembl
chr7:102555712..102556806hg19UCSC Ensembl
Innerchr7:102555737..102556781hg19UCSC Ensembl
Outerchr7:102555687..102556831hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12912187
SamplesHG01431
Known GenesFBXL13, LRRC17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614365
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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