A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126918



Internal ID15633418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9794545..9851382hg38UCSC Ensembl
Innerchr9:9794545..9851382hg19UCSC Ensembl
Innerchr9:9784545..9841382hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3856838
hg1956838
hg1856838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613327
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126918
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