A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614834



Internal ID16402243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89487669..89511100hg38UCSC Ensembl
Innerchr9:92102584..92126015hg19UCSC Ensembl
Innerchr9:91292404..91315835hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3823432
hg1923432
hg1823432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139229
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614834
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