A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571042



Internal ID16011765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:785298..847566hg38UCSC Ensembl
Innerchr16:835298..897566hg19UCSC Ensembl
Innerchr16:775299..837567hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3862269
hg1962269
hg1862269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv851854
Samples
Known GenesCHTF18, GNG13, PRR25, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571042
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