A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617995



Internal ID7004878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90291326..90295306hg38UCSC Ensembl
Innerchr8:90291333..90295300hg38UCSC Ensembl
Outerchr8:90291320..90295313hg38UCSC Ensembl
chr8:91303554..91307534hg19UCSC Ensembl
Innerchr8:91303561..91307528hg19UCSC Ensembl
Outerchr8:91303548..91307541hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383981
hg193981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13253780
SamplesNA20859
Known GenesLINC00534
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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