A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610103



Internal ID6997022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98167595..98186744hg38UCSC Ensembl
Innerchr6:98167611..98186728hg38UCSC Ensembl
Outerchr6:98167579..98186760hg38UCSC Ensembl
chr6:98615471..98634620hg19UCSC Ensembl
Innerchr6:98615487..98634604hg19UCSC Ensembl
Outerchr6:98615455..98634636hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3819150
hg1919150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12475106
SamplesHG02982
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610103
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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