A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3345365



Internal ID15192349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71058938..71058957hg38UCSC Ensembl
Innerchr15:71058934..71058961hg38UCSC Ensembl
Outerchr15:71058915..71058980hg38UCSC Ensembl
chr15:71351277..71351296hg19UCSC Ensembl
Innerchr15:71351273..71351300hg19UCSC Ensembl
Outerchr15:71351254..71351319hg19UCSC Ensembl
chr15:69138331..69138350hg18UCSC Ensembl
Innerchr15:69138354..69138327hg18UCSC Ensembl
Outerchr15:69138308..69138373hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9669524
SamplesNA11894
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3345365
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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