A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048832



Internal ID19138051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22095238hg38UCSC Ensembl
Innerchr15:20585976..22383189hg19UCSC Ensembl
Innerchr15:18845990..19884553hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381714516
hg191797214
hg181038564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2213n100
Supporting Variantsnssv3537361, nssv3537362
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1048832
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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