A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618675



Internal ID6658869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123975694..124011585hg38UCSC Ensembl
Innerchr8:123975694..124011585hg38UCSC Ensembl
Outerchr8:123975194..124012085hg38UCSC Ensembl
chr8:124987934..125023825hg19UCSC Ensembl
Innerchr8:124987934..125023825hg19UCSC Ensembl
Outerchr8:124987434..125024325hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3835892
hg1935892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13310537
SamplesHG01515
Known GenesFER1L6, FER1L6-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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