A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618044



Internal ID7004927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92797388..92798609hg38UCSC Ensembl
Innerchr8:92797399..92798598hg38UCSC Ensembl
Outerchr8:92797377..92798620hg38UCSC Ensembl
chr8:93809616..93810837hg19UCSC Ensembl
Innerchr8:93809627..93810826hg19UCSC Ensembl
Outerchr8:93809605..93810848hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13258154
SamplesHG02325
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618044
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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