A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4009985



Internal ID22071616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86240009..86258687hg38UCSC Ensembl
Outerchr16:86232426..86268426hg38UCSC Ensembl
Innerchr16:86273615..86292293hg19UCSC Ensembl
Outerchr16:86266032..86302032hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3836001
hg1936001
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155364
Supporting Variants
Samples
Known GenesLINC01081
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4009985
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer