A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615828



Internal ID7002716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1392031..1462882hg38UCSC Ensembl
Innerchr8:1392531..1462382hg38UCSC Ensembl
Outerchr8:1391031..1463882hg38UCSC Ensembl
chr8:1340197..1411048hg19UCSC Ensembl
Innerchr8:1340697..1410548hg19UCSC Ensembl
Outerchr8:1339197..1412048hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3870852
hg1970852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1354e214
Supporting Variantsessv13060079
SamplesHG03720
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615828
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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