A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1776



Internal ID15199653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28651037..28796959hg38UCSC Ensembl
Outerchr16:28662358..28808280hg19UCSC Ensembl
Outerchr16:28569859..28715781hg18UCSC Ensembl
Outerchr16:28569859..28715781hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38145923
hg19145923
hg18145923
hg17145923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2139
SamplesNA18555
Known GenesEIF3C, EIF3CL, MIR6862-1, MIR6862-2
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv1776
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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