A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054353



Internal ID18796884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34563605hg38UCSC Ensembl
Innerchr15:34695310..34855806hg19UCSC Ensembl
Innerchr15:32482602..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38160497
hg19160497
hg18160497
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2559n100
Supporting Variantsnssv3548760, nssv3548751, nssv3548763, nssv3548757, nssv3548762, nssv3548764, nssv3548752, nssv3721715, nssv3721713, nssv3548761, nssv3548750, nssv3721718, nssv3548753, nssv3548758, nssv3721717, nssv3548754, nssv3548755, nssv3548759, nssv3721716, nssv3721720, nssv3721714, nssv3721719, nssv3548756
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054353
Frequency
Sample Size29084
Observed Gain3
Observed Loss20
Observed Complex0
Frequencyn/a


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