A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1132841



Internal ID15986027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33445718..33447826hg38UCSC Ensembl
Innerchr9:33445716..33447824hg19UCSC Ensembl
Innerchr9:33435716..33437824hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382109
hg192109
hg182109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614149
Supporting Variants
Samples
Known GenesAQP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1132841
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