A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8968273



Internal ID14389265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53161413..53161425hg38UCSC Ensembl
Innerchr15:53161404..53161431hg38UCSC Ensembl
Outerchr15:53161392..53161446hg38UCSC Ensembl
chr15:53453610..53453622hg19UCSC Ensembl
Innerchr15:53453601..53453628hg19UCSC Ensembl
Outerchr15:53453589..53453643hg19UCSC Ensembl
chr15:51240902..51240914hg18UCSC Ensembl
Innerchr15:51240920..51240893hg18UCSC Ensembl
Outerchr15:51240881..51240935hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38283
hg19283
hg18283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3388451
Supporting Variants
SamplesNA18870
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8968273
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer