A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049109



Internal ID19138328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20210878..20929146hg38UCSC Ensembl
Innerchr15:20416131..21134475hg19UCSC Ensembl
Innerchr15:18676145..19399134hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38718269
hg19718345
hg18722990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2211n100
Supporting Variantsnssv3538216
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1049109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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