A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035467



Internal ID19124686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376186..20844186hg38UCSC Ensembl
Innerchr15:20581439..21049515hg19UCSC Ensembl
Innerchr15:18841453..19314115hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38468001
hg19468077
hg18472663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2245n100
Supporting Variantsnssv3714560
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, 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)nsv1035467
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