A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617858



Internal ID7004742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84515845..84528871hg38UCSC Ensembl
Innerchr8:84515995..84528721hg38UCSC Ensembl
Outerchr8:84515695..84529021hg38UCSC Ensembl
chr8:85428080..85441106hg19UCSC Ensembl
Innerchr8:85428230..85440956hg19UCSC Ensembl
Outerchr8:85427930..85441256hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3813027
hg1913027
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13243954
SamplesHG01617
Known GenesRALYL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617858
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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