A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852081



Internal ID15799351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1989307..2264400hg38UCSC Ensembl
Innerchr16:2039308..2314401hg19UCSC Ensembl
Innerchr16:1979309..2254402hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38275094
hg19275094
hg18275094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571188
Supporting Variants
Samples
Known GenesBRICD5, CASKIN1, DNASE1L2, E4F1, ECI1, MIR1225, MIR3180-5, MIR4516, MIR6511B-1, MLST8, NPW, NTHL1, PGP, PKD1, RAB26, RNPS1, SLC9A3R2, SNORD60, SYNGR3, TRAF7, TSC2, ZNF598
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852081
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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