A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670459



Internal ID15407111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79977418..79987809hg38UCSC Ensembl
Innerchr9:82592333..82602724hg19UCSC Ensembl
Innerchr9:81782153..81792544hg18UCSC Ensembl
Innerchr9:79821887..79832278hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3810392
hg1910392
hg1810392
hg1710392
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516724
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670459
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