A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695077



Internal ID15085043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114309648..114311045hg38UCSC Ensembl
Innerchr9:117071928..117073325hg19UCSC Ensembl
Innerchr9:116111749..116113146hg18UCSC Ensembl
Innerchr9:114151482..114152879hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381398
hg191398
hg181398
hg171398
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522296
Supporting Variants
Samples
Known GenesCOL27A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695077
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