A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689142



Internal ID18640737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9776126..10481262hg38UCSC Ensembl
Innerchr9:9776126..10481262hg19UCSC Ensembl
Innerchr9:9766126..10471262hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38705137
hg19705137
hg18705137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034731
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)nssv3689142
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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