A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3437782



Internal ID15284735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37708176..37710474hg38UCSC Ensembl
Innerchr8:37709176..37709474hg38UCSC Ensembl
Outerchr8:37707176..37711474hg38UCSC Ensembl
chr8:37565694..37567992hg19UCSC Ensembl
Innerchr8:37566694..37566992hg19UCSC Ensembl
Outerchr8:37564694..37568992hg19UCSC Ensembl
chr8:37684852..37687150hg18UCSC Ensembl
Innerchr8:37685852..37686150hg18UCSC Ensembl
Outerchr8:37683852..37688150hg18UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696289
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3437782
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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