A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704838



Internal ID15441490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132213867..132216219hg38UCSC Ensembl
Innerchr9:135089254..135091606hg19UCSC Ensembl
Innerchr9:134079075..134081427hg18UCSC Ensembl
Innerchr9:132118808..132121160hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382353
hg192353
hg182353
hg172353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528270
Supporting Variants
Samples
Known GenesNTNG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704838
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