A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989760



Internal ID12975050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25440278..25538778hg38UCSC Ensembl
Innerchr11:25461824..25560324hg19UCSC Ensembl
Innerchr11:25418400..25516900hg18UCSC Ensembl
Innerchr11:25418400..25516900hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3898501
hg1998501
hg1898501
hg1798501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751021
Supporting Variants
SamplesBEC_558
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989760
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