A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571539



Internal ID16012262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15856272..15856892hg38UCSC Ensembl
Innerchr16:15950129..15950749hg19UCSC Ensembl
Innerchr16:15857630..15858250hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38621
hg19621
hg18621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4925n54
Supporting Variantsnssv852818
Samples
Known GenesMYH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571539
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