A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025791



Internal ID19115008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9294304..9626331hg38UCSC Ensembl
Innerchr9:9294304..9626331hg19UCSC Ensembl
Innerchr9:9284304..9616331hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38332028
hg19332028
hg18332028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689127
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)nsv1025791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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