A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033178



Internal ID19122400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10169848..10428731hg38UCSC Ensembl
Innerchr9:10169848..10428731hg19UCSC Ensembl
Innerchr9:10159848..10418731hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38258884
hg19258884
hg18258884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758152
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)nsv1033178
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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