A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8672137



Internal ID15106897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61377726..61377738hg38UCSC Ensembl
Innerchr11:61377717..61377747hg38UCSC Ensembl
Outerchr11:61377703..61377759hg38UCSC Ensembl
chr11:61145198..61145210hg19UCSC Ensembl
Innerchr11:61145189..61145219hg19UCSC Ensembl
Outerchr11:61145175..61145231hg19UCSC Ensembl
chr11:60901774..60901786hg18UCSC Ensembl
Innerchr11:60901795..60901765hg18UCSC Ensembl
Outerchr11:60901751..60901807hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38251
hg19251
hg18251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3396361
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8672137
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