A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952908



Internal ID16955095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3462801..3499000hg38UCSC Ensembl
Outerchr16:3512801..3549000hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3836200
hg1936200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999204
SamplesBILGI_BIOE
Known GenesC16orf90, MIR6126, NAA60
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952908
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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