A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012480



Internal ID19101697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10689974..10706394hg38UCSC Ensembl
Innerchr4:10691598..10708018hg19UCSC Ensembl
Innerchr4:10300696..10317116hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3816421
hg1916421
hg1816421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3619744
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)nsv1012480
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