A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451382



Internal ID15298328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28216411..28217609hg38UCSC Ensembl
Innerchr15:28216609..28217411hg38UCSC Ensembl
Outerchr15:28215411..28218609hg38UCSC Ensembl
chr15:28461557..28462755hg19UCSC Ensembl
Innerchr15:28461755..28462557hg19UCSC Ensembl
Outerchr15:28460557..28463755hg19UCSC Ensembl
chr15:26135152..26136350hg18UCSC Ensembl
Innerchr15:26136152..26135350hg18UCSC Ensembl
Outerchr15:26134152..26137350hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8689719
SamplesNA19240
Known GenesHERC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451382
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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