A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052868



Internal ID18795399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34520906hg38UCSC Ensembl
Innerchr15:34695310..34813107hg19UCSC Ensembl
Innerchr15:32482602..32600399hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38117798
hg19117798
hg18117798
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2558n100
Supporting Variantsnssv3548666, nssv3721682, nssv3548668, nssv3548667, nssv3548664, nssv3548665, nssv3721681
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052868
Frequency
Sample Size29084
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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