A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618679



Internal ID7005561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124074644..124077403hg38UCSC Ensembl
Innerchr8:124074660..124077387hg38UCSC Ensembl
Outerchr8:124074628..124077419hg38UCSC Ensembl
chr8:125086885..125089644hg19UCSC Ensembl
Innerchr8:125086901..125089628hg19UCSC Ensembl
Outerchr8:125086869..125089660hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg382760
hg192760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13310731
SamplesHG03781
Known GenesFER1L6, FER1L6-AS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618679
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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