A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613385



Internal ID16400794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10427780..10468666hg38UCSC Ensembl
Innerchr9:10427780..10468666hg19UCSC Ensembl
Innerchr9:10417780..10458666hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3840887
hg1940887
hg1840887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128509
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613385
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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