A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704738



Internal ID15094704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4267209..4272449hg38UCSC Ensembl
Innerchr9:4267209..4272449hg19UCSC Ensembl
Innerchr9:4257209..4262449hg18UCSC Ensembl
Innerchr9:4257209..4262449hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg385241
hg195241
hg185241
hg175241
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520350
Supporting Variants
Samples
Known GenesGLIS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704738
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