A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990386



Internal ID12980461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152707769..152770328hg38UCSC Ensembl
Innerchr3:152425558..152488117hg19UCSC Ensembl
Innerchr3:153908248..153970807hg18UCSC Ensembl
Innerchr3:153908256..153970815hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3862560
hg1962560
hg1862560
hg1762560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34910
Supporting Variants
SamplesNA18579
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990386
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