A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018814



Internal ID18761347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9793285..9957301hg38UCSC Ensembl
Innerchr9:9793285..9957301hg19UCSC Ensembl
Innerchr9:9783285..9947301hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38164017
hg19164017
hg18164017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758129
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)nsv1018814
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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