A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054887



Internal ID19144106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..20681492hg38UCSC Ensembl
Innerchr15:20590015..20886821hg19UCSC Ensembl
Innerchr15:18850029..19146835hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38296731
hg19296807
hg18296807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2244n100
Supporting Variantsnssv3714771
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054887
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