A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045946



Internal ID18788477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82652403..82886826hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg18234424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2638n100
Supporting Variantsnssv3554673
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045946
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