A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047090



Internal ID18789621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90301813..90400239hg38UCSC Ensembl
Innerchr15:90845045..90943471hg19UCSC Ensembl
Innerchr15:88646049..88744475hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3898427
hg1998427
hg1898427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2659n100
Supporting Variantsnssv3555207
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047090
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