A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3367446



Internal ID15214422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105908489..105908524hg38UCSC Ensembl
Innerchr8:105908501..105908512hg38UCSC Ensembl
Outerchr8:105908477..105908536hg38UCSC Ensembl
chr8:106920717..106920752hg19UCSC Ensembl
Innerchr8:106920729..106920740hg19UCSC Ensembl
Outerchr8:106920705..106920764hg19UCSC Ensembl
chr8:106989893..106989928hg18UCSC Ensembl
Innerchr8:106989905..106989916hg18UCSC Ensembl
Outerchr8:106989881..106989940hg18UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38263
hg19263
hg18263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8676920
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3367446
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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