A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615874



Internal ID16403283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135375724..135472087hg38UCSC Ensembl
Innerchr9:138267570..138363933hg19UCSC Ensembl
Innerchr9:137407391..137503754hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3896364
hg1996364
hg1896364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1147124
Samples
Known GenesPPP1R26-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615874
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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