A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615216



Internal ID16055939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113594236..113633818hg38UCSC Ensembl
Innerchr9:116356516..116396098hg19UCSC Ensembl
Innerchr9:115396337..115435919hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3839583
hg1939583
hg1839583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12854n54
Supporting Variantsnssv1141258
Samples
Known GenesRGS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615216
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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