A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569160



Internal ID16356569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35729419..36021764hg38UCSC Ensembl
Innerchr15:36021620..36313965hg19UCSC Ensembl
Innerchr15:33808912..34101257hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38292346
hg19292346
hg18292346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149154
Samples1780854279_A
Known GenesDPH6-AS1, MIR4510
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569160
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