A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617435



Internal ID7004320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63923058..63939063hg38UCSC Ensembl
Innerchr8:63923062..63939059hg38UCSC Ensembl
Outerchr8:63923054..63939067hg38UCSC Ensembl
chr8:64835615..64851620hg19UCSC Ensembl
Innerchr8:64835619..64851616hg19UCSC Ensembl
Outerchr8:64835611..64851624hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3816006
hg1916006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1401e214
Supporting Variantsessv13213166, essv13213167, essv13213168
SamplesHG03172, NA18510, NA19131
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617435
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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