A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616016



Internal ID16056739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137200153..137318190hg38UCSC Ensembl
Innerchr9:140094605..140212642hg19UCSC Ensembl
Innerchr9:139214426..139332463hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38118038
hg19118038
hg18118038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13009n54
Supporting Variantsnssv1148371
Samples
Known GenesC9orf169, C9orf173, EXD3, FAM166A, LOC100129722, NDOR1, NELFB, NRARP, RNF208, RNF224, SLC34A3, TMEM203, TOR4A, TPRN, TUBB4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616016
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