A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694171



Internal ID15084137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9862074..9862312hg38UCSC Ensembl
Innerchr4:9863698..9863936hg19UCSC Ensembl
Innerchr4:9472796..9473034hg18UCSC Ensembl
Innerchr4:9539967..9540205hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38239
hg19239
hg18239
hg17239
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519519
Supporting Variants
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer