A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3417795



Internal ID15264753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68487707..68487716hg38UCSC Ensembl
Innerchr15:68487691..68487732hg38UCSC Ensembl
Outerchr15:68487682..68487741hg38UCSC Ensembl
chr15:68780046..68780055hg19UCSC Ensembl
Innerchr15:68780030..68780071hg19UCSC Ensembl
Outerchr15:68780021..68780080hg19UCSC Ensembl
chr15:66567100..66567109hg18UCSC Ensembl
Innerchr15:66567125..66567084hg18UCSC Ensembl
Outerchr15:66567075..66567134hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865821
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3417795
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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