A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569322



Internal ID16356731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:46801652..46852188hg38UCSC Ensembl
Innerchr15:47093850..47144386hg19UCSC Ensembl
Innerchr15:44881142..44931678hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3850537
hg1950537
hg1850537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149593
Samples1780854449_A
Known GenesMIR548A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569322
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