A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979607



Internal ID12980452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152707513..152770513hg38UCSC Ensembl
Innerchr3:152425302..152488302hg19UCSC Ensembl
Innerchr3:153907992..153970992hg18UCSC Ensembl
Innerchr3:153908000..153971000hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3863001
hg1963001
hg1863001
hg1763001
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)essv6979607
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