A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571185



Internal ID16011908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1971892..2246850hg38UCSC Ensembl
Innerchr16:2021893..2296851hg19UCSC Ensembl
Innerchr16:1961894..2236852hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38274959
hg19274959
hg18274959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4859n54
Supporting Variantsnssv852078
Samples
Known GenesBRICD5, CASKIN1, DNASE1L2, E4F1, ECI1, GFER, MIR1225, MIR3180-5, MIR4516, MIR6511B-1, MLST8, NOXO1, NPW, NTHL1, PGP, PKD1, RAB26, SLC9A3R2, SNORD60, SYNGR3, TBL3, TRAF7, TSC2, ZNF598
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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