A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617424



Internal ID6657619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63202669..63204567hg38UCSC Ensembl
Innerchr8:63202669..63204567hg38UCSC Ensembl
Outerchr8:63202418..63204805hg38UCSC Ensembl
chr8:64115227..64117125hg19UCSC Ensembl
Innerchr8:64115227..64117125hg19UCSC Ensembl
Outerchr8:64114976..64117363hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13213086
SamplesNA18950
Known GenesYTHDF3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617424
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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