A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983673



Internal ID12629070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8425646..8650000hg38UCSC Ensembl
Innerchr11:8447193..8671547hg19UCSC Ensembl
Innerchr11:8403769..8628123hg18UCSC Ensembl
Innerchr11:8403769..8628123hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38224355
hg19224355
hg18224355
hg17224355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751035
Supporting Variants
SamplesBEC_611
Known GenesSTK33, TRIM66
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983673
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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