A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1145117



Internal ID15998303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130154956..130232881hg38UCSC Ensembl
Innerchr9:132917235..132995160hg19UCSC Ensembl
Innerchr9:131957056..132034981hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3877926
hg1977926
hg1877926
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615499
Supporting Variants
Samples
Known GenesNCS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1145117
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