A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618060



Internal ID6658255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93645500..93647220hg38UCSC Ensembl
Innerchr8:93645500..93647220hg38UCSC Ensembl
Outerchr8:93645284..93647444hg38UCSC Ensembl
chr8:94657728..94659448hg19UCSC Ensembl
Innerchr8:94657728..94659448hg19UCSC Ensembl
Outerchr8:94657512..94659672hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381721
hg191721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13260195
SamplesNA18542
Known GenesLINC00535
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618060
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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