A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051089



Internal ID19140308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..22153784hg38UCSC Ensembl
Innerchr15:20284054..22441735hg19UCSC Ensembl
Innerchr15:18544068..19943099hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382074984
hg192157682
hg181399032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n100
Supporting Variantsnssv3716010
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051089
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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