A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570924



Internal ID16011647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84458..102222hg38UCSC Ensembl
Innerchr16:134457..152220hg19UCSC Ensembl
Innerchr16:74457..92220hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817765
hg1917764
hg1817764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851235
Samples
Known GenesMPG, NPRL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570924
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