A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657785



Internal ID9577204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:28597631..28609045hg38UCSC Ensembl
Outerchr8:28597474..28609198hg38UCSC Ensembl
Innerchr8:28455148..28466562hg19UCSC Ensembl
Outerchr8:28454991..28466715hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3811725
hg1911725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6504653
SamplesHG00325
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657785
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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