A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024452



Internal ID19113669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9339770..9355896hg38UCSC Ensembl
Innerchr9:9339770..9355896hg19UCSC Ensembl
Innerchr9:9329770..9345896hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3816127
hg1916127
hg1816127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689128
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)nsv1024452
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