A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614364



Internal ID7001258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102907003..102914116hg38UCSC Ensembl
Innerchr7:102907008..102914111hg38UCSC Ensembl
Outerchr7:102906998..102914121hg38UCSC Ensembl
chr7:102547450..102554563hg19UCSC Ensembl
Innerchr7:102547455..102554558hg19UCSC Ensembl
Outerchr7:102547445..102554568hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387114
hg197114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12912186
SamplesHG01872
Known GenesFBXL13, LRRC17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614364
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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