A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568310



Internal ID16355719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23403645..23474682hg38UCSC Ensembl
Innerchr15:23648792..23719829hg19UCSC Ensembl
Innerchr15:21200233..21270922hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3871038
hg1971038
hg1870690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148658
SamplesHGDP01330
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568310
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