A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028702



Internal ID19117920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10439300..10502638hg38UCSC Ensembl
Innerchr9:10439300..10502638hg19UCSC Ensembl
Innerchr9:10429300..10492638hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3863339
hg1963339
hg1863339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7405n100
Supporting Variantsnssv3689187
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)nsv1028702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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