A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984070



Internal ID12630975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:62012550..62078514hg38UCSC Ensembl
Innerchr11:61780022..61845986hg19UCSC Ensembl
Innerchr11:61536598..61602562hg18UCSC Ensembl
Innerchr11:61536598..61602562hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3865965
hg1965965
hg1865965
hg1765965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751033
Supporting Variants
SamplesBEC_768
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984070
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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