A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061733



Internal ID18804264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18464130..18568345hg38UCSC Ensembl
Innerchr19:18574940..18679155hg19UCSC Ensembl
Innerchr19:18435940..18540155hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38104216
hg19104216
hg18104216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3569783
Samples
Known GenesELL, FKBP8, KXD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061733
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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