A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126884



Internal ID15980070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8573166..8615045hg38UCSC Ensembl
Innerchr9:8573166..8615045hg19UCSC Ensembl
Innerchr9:8563166..8605045hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841880
hg1941880
hg1841880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613291
Supporting Variants
Samples
Known GenesPTPRD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126884
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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