A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032936



Internal ID19122158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10541177..10633543hg38UCSC Ensembl
Innerchr9:10541177..10633543hg19UCSC Ensembl
Innerchr9:10531177..10623543hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3892367
hg1992367
hg1892367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689188
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)nsv1032936
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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