A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3375746



Internal ID15222721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882878..82882883hg38UCSC Ensembl
chr15:83551630..83557686hg19UCSC Ensembl
Innerchr15:83551622..83557694hg19UCSC Ensembl
Outerchr15:83551616..83557700hg19UCSC Ensembl
chr15:81348684..81348690hg18UCSC Ensembl
Innerchr15:81348698..81348676hg18UCSC Ensembl
Outerchr15:81348670..81348704hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386032
hg196032
hg186032
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8673254, essv8673251, essv8673252
SamplesNA19239, NA12892, NA19240
Known GenesHOMER2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3375746
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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