A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689123



Internal ID18987404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8929663..9011443hg38UCSC Ensembl
Innerchr9:8929663..9011443hg19UCSC Ensembl
Innerchr9:8919663..9001443hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3881781
hg1981781
hg1881781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021214
Supporting Variants
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)nssv3689123
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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