A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009520



Internal ID18752051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12160505..12270788hg38UCSC Ensembl
Innerchr4:12162129..12272412hg19UCSC Ensembl
Innerchr4:11771227..11881510hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38110284
hg19110284
hg18110284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737698
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)nsv1009520
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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