A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3558035



Internal ID18509630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16283793..16704794hg38UCSC Ensembl
Innerchr16:16377650..16798651hg19UCSC Ensembl
Innerchr16:16285151..16706152hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38421002
hg19421002
hg18421002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047549
Supporting Variants
Samples
Known GenesLOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO3, NPIPA7, NPIPA8, PKD1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3558035
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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