A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610108



Internal ID6997027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98670826..98694136hg38UCSC Ensembl
Innerchr6:98670836..98694126hg38UCSC Ensembl
Outerchr6:98670816..98694146hg38UCSC Ensembl
chr6:99118702..99142012hg19UCSC Ensembl
Innerchr6:99118712..99142002hg19UCSC Ensembl
Outerchr6:99118692..99142022hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3823311
hg1923311
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12475266
SamplesNA12144
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610108
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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