A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616841



Internal ID7003727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33644093..33673212hg38UCSC Ensembl
Innerchr8:33644593..33672712hg38UCSC Ensembl
Outerchr8:33643093..33674212hg38UCSC Ensembl
chr8:33501611..33530730hg19UCSC Ensembl
Innerchr8:33502111..33530230hg19UCSC Ensembl
Outerchr8:33500611..33531730hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3829120
hg1929120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13161530, essv13161532, essv13161531, essv13161527, essv13161529, essv13161528
SamplesHG01098, NA19782, HG01405, NA19732, HG00734, HG01061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616841
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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