A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569804



Internal ID16357213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:67874592..67940161hg38UCSC Ensembl
Innerchr15:68166930..68232499hg19UCSC Ensembl
Innerchr15:65953984..66019553hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3865570
hg1965570
hg1865570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844364
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569804
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