A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569982



Internal ID16010705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74417784..74429628hg38UCSC Ensembl
Innerchr15:74710125..74721969hg19UCSC Ensembl
Innerchr15:72497178..72509022hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3811845
hg1911845
hg1811845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845276
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569982
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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