A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3410982



Internal ID15257942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58502511..58502522hg38UCSC Ensembl
Innerchr15:58502513..58502520hg38UCSC Ensembl
Outerchr15:58502509..58502524hg38UCSC Ensembl
chr15:58794710..58794721hg19UCSC Ensembl
Innerchr15:58794712..58794719hg19UCSC Ensembl
Outerchr15:58794708..58794723hg19UCSC Ensembl
chr15:56582002..56582013hg18UCSC Ensembl
Innerchr15:56582004..56582011hg18UCSC Ensembl
Outerchr15:56582000..56582015hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865814
SamplesNA12005
Known GenesLIPC
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3410982
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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