A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682410



Internal ID15419062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101880684..102142172hg38UCSC Ensembl
Innerchr9:104642966..104904454hg19UCSC Ensembl
Innerchr9:103682787..103944275hg18UCSC Ensembl
Innerchr9:101722521..101984009hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38261489
hg19261489
hg18261489
hg17261489
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521116
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682410
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