A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009488



Internal ID19098706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12340473..12363374hg38UCSC Ensembl
Innerchr4:12342097..12364998hg19UCSC Ensembl
Innerchr4:11951195..11974096hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3822902
hg1922902
hg1822902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619760
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009488
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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