A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615229



Internal ID16055952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114145273..114167914hg38UCSC Ensembl
Innerchr9:116907553..116930194hg19UCSC Ensembl
Innerchr9:115947374..115970015hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3822642
hg1922642
hg1822642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12857n54
Supporting Variantsnssv1176468
SamplesNINDS_49
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615229
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