A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030899



Internal ID19120119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9250314..9291197hg38UCSC Ensembl
Innerchr9:9250314..9291197hg19UCSC Ensembl
Innerchr9:9240314..9281197hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3840884
hg1940884
hg1840884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689126
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)nsv1030899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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