A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617506



Internal ID7004391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67582144..67607325hg38UCSC Ensembl
Innerchr8:67582159..67607310hg38UCSC Ensembl
Outerchr8:67582129..67607340hg38UCSC Ensembl
chr8:68494379..68519560hg19UCSC Ensembl
Innerchr8:68494394..68519545hg19UCSC Ensembl
Outerchr8:68494364..68519575hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3825182
hg1925182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13216304
SamplesHG04235
Known GenesCPA6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617506
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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