A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618110



Internal ID7004993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95746056..95759375hg38UCSC Ensembl
Innerchr8:95746056..95759375hg38UCSC Ensembl
Outerchr8:95745556..95759875hg38UCSC Ensembl
chr8:96758284..96771603hg19UCSC Ensembl
Innerchr8:96758284..96771603hg19UCSC Ensembl
Outerchr8:96757784..96772103hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3813320
hg1913320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13263887
SamplesHG03019
Known GenesLOC100616530
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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