A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695913



Internal ID15432565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3971303..3973853hg38UCSC Ensembl
Innerchr9:3971303..3973853hg19UCSC Ensembl
Innerchr9:3961303..3963853hg18UCSC Ensembl
Innerchr9:3961303..3963853hg17UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg382551
hg192551
hg182551
hg172551
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518476
Supporting Variants
Samples
Known GenesGLIS3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695913
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