A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980171



Internal ID12981373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104436213..105058446hg38UCSC Ensembl
Innerchr3:104155057..104777290hg19UCSC Ensembl
Innerchr3:105637747..106259980hg18UCSC Ensembl
Innerchr3:105637747..106259980hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38622234
hg19622234
hg18622234
hg17622234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35023
Supporting Variants
SamplesNA18966
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980171
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