A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047063



Internal ID19136282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..22472558hg38UCSC Ensembl
Innerchr15:20586733..22751770hg19UCSC Ensembl
Innerchr15:18846747..20303134hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382091079
hg192165038
hg181456388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2183n100
Supporting Variantsnssv3539533
Samples
Known GenesCT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, 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)nsv1047063
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