A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021264



Internal ID19110481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22159623..22293805hg38UCSC Ensembl
Innerchr9:22159622..22293804hg19UCSC Ensembl
Innerchr9:22149622..22283804hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38134183
hg19134183
hg18134183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690721
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)nsv1021264
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