A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049808



Internal ID18792339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137356366..137438026hg38UCSC Ensembl
Innerchr9:140250818..140332478hg19UCSC Ensembl
Innerchr9:139370639..139452299hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3881661
hg1981661
hg1881661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759864
Samples
Known GenesENTPD8, EXD3, NOXA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049808
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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