A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434189



Internal ID15281143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40343777..40343796hg38UCSC Ensembl
Innerchr15:40343773..40343800hg38UCSC Ensembl
Outerchr15:40343754..40343819hg38UCSC Ensembl
chr15:40635978..40635997hg19UCSC Ensembl
Innerchr15:40635974..40636001hg19UCSC Ensembl
Outerchr15:40635955..40636020hg19UCSC Ensembl
chr15:38423270..38423289hg18UCSC Ensembl
Innerchr15:38423293..38423266hg18UCSC Ensembl
Outerchr15:38423247..38423312hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9668269
SamplesNA18970
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434189
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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