A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051866



Internal ID18794397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34447659..34740872hg38UCSC Ensembl
Innerchr15:34739860..35033073hg19UCSC Ensembl
Innerchr15:32527152..32820365hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38293214
hg19293214
hg18293214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2571n100
Supporting Variantsnssv3552107
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051866
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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