A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016118



Internal ID19105336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9444744..9582169hg38UCSC Ensembl
Innerchr9:9444744..9582169hg19UCSC Ensembl
Innerchr9:9434744..9572169hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38137426
hg19137426
hg18137426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689138
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)nsv1016118
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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