A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033404



Internal ID19122626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9058285..9211223hg38UCSC Ensembl
Innerchr9:9058285..9211223hg19UCSC Ensembl
Innerchr9:9048285..9201223hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38152939
hg19152939
hg18152939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689125
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033404
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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