A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615232



Internal ID16055955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114167820..114195678hg38UCSC Ensembl
Innerchr9:116930100..116957958hg19UCSC Ensembl
Innerchr9:115969921..115997779hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3827859
hg1927859
hg1827859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141263
Samples
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615232
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