A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568748



Internal ID16009471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30562104..30670617hg38UCSC Ensembl
Innerchr15:30854307..30962820hg19UCSC Ensembl
Innerchr15:28641599..28750112hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38108514
hg19108514
hg18108514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839477
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568748
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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