A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681109



Internal ID15071075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5460910..5464065hg38UCSC Ensembl
Innerchr9:5460910..5464065hg19UCSC Ensembl
Innerchr9:5450910..5454065hg18UCSC Ensembl
Innerchr9:5450910..5454065hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg383156
hg193156
hg183156
hg173156
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519771
Supporting Variants
Samples
Known GenesCD274
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681109
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