A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044828



Internal ID18787359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22635932..23226874hg38UCSC Ensembl
Innerchr15:22582517..23237164hg19UCSC Ensembl
Innerchr15:20083881..20788605hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38590943
hg19654648
hg18704725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2403n100
Supporting Variantsnssv3538809
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044828
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