A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695799



Internal ID15085765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91795844..91843626hg38UCSC Ensembl
Innerchr9:94558126..94605908hg19UCSC Ensembl
Innerchr9:93597947..93645729hg18UCSC Ensembl
Innerchr9:91637681..91685463hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3847783
hg1947783
hg1847783
hg1747783
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518372
Supporting Variants
Samples
Known GenesROR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695799
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