A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568770



Internal ID16009493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31064222..31102334hg38UCSC Ensembl
Innerchr15:31356425..31394537hg19UCSC Ensembl
Innerchr15:29143717..29181829hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3838113
hg1938113
hg1838113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4428n54
Supporting Variantsnssv839500
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568770
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