A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852263



Internal ID15799533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3563125..3589138hg38UCSC Ensembl
Innerchr16:3613126..3639139hg19UCSC Ensembl
Innerchr16:3553127..3579140hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3826014
hg1926014
hg1826014
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571255
Supporting Variants
Samples
Known GenesNLRC3, SLX4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852263
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