A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700369



Internal ID15437021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11753695..12096410hg38UCSC Ensembl
Innerchr9:11753695..12096410hg19UCSC Ensembl
Innerchr9:11743695..12086410hg18UCSC Ensembl
Innerchr9:11743695..12086410hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38342716
hg19342716
hg18342716
hg17342716
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700369
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