A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613378



Internal ID16400787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10365060..10557349hg38UCSC Ensembl
Innerchr9:10365060..10557349hg19UCSC Ensembl
Innerchr9:10355060..10547349hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38192290
hg19192290
hg18192290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156250
SamplesHGDP01332
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613378
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