A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615196



Internal ID16055919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112305317..112382301hg38UCSC Ensembl
Innerchr9:115067597..115144581hg19UCSC Ensembl
Innerchr9:114107418..114184402hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3876985
hg1976985
hg1876985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176120
SamplesNINDS_272
Known GenesHSDL2, MIR3134, PTBP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615196
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer