A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050281



Internal ID19139500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30360018hg38UCSC Ensembl
Innerchr15:30493349..30652221hg19UCSC Ensembl
Innerchr15:28280641..28439513hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38158873
hg19158873
hg18158873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2501n100
Supporting Variantsnssv3546567
Samples
Known GenesDKFZP434L187
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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