A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618079



Internal ID7004962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94571903..94582827hg38UCSC Ensembl
Innerchr8:94571903..94582827hg38UCSC Ensembl
Outerchr8:94571403..94583327hg38UCSC Ensembl
chr8:95584131..95595055hg19UCSC Ensembl
Innerchr8:95584131..95595055hg19UCSC Ensembl
Outerchr8:95583631..95595555hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3810925
hg1910925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13260633
SamplesNA12874
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618079
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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