A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024788



Internal ID19114005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:31164391..31251580hg38UCSC Ensembl
Innerchr9:31164389..31251578hg19UCSC Ensembl
Innerchr9:31154389..31241578hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3887190
hg1987190
hg1887190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7509n100
Supporting Variantsnssv3688845
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer