A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569817



Internal ID16010540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70939166..71145216hg38UCSC Ensembl
Innerchr15:71231505..71437555hg19UCSC Ensembl
Innerchr15:69018559..69224609hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38206051
hg19206051
hg18206051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844373
Samples
Known GenesCT62, LRRC49, THSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569817
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