A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852519



Internal ID16146475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9663449..9705784hg38UCSC Ensembl
Innerchr16:9757306..9799641hg19UCSC Ensembl
Innerchr16:9664807..9707142hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3842336
hg1942336
hg1842336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571440
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852519
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