A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683908



Internal ID15073874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29927529..29933215hg38UCSC Ensembl
Innerchr9:29927527..29933213hg19UCSC Ensembl
Innerchr9:29917527..29923213hg18UCSC Ensembl
Innerchr9:29917527..29923213hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385687
hg195687
hg185687
hg175687
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683908
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