A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015319



Internal ID19104536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13931837..13970420hg38UCSC Ensembl
Innerchr9:13931836..13970419hg19UCSC Ensembl
Innerchr9:13921836..13960419hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3838584
hg1938584
hg1838584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758232
Samples
Known GenesLINC00583
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015319
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