A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047580



Internal ID19136799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22283155hg38UCSC Ensembl
Innerchr15:20585976..22571106hg19UCSC Ensembl
Innerchr15:18845990..20072470hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381902433
hg191985131
hg181226481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3714675
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047580
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