A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557539



Internal ID18509134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..14969848hg38UCSC Ensembl
Innerchr16:14888583..15063705hg19UCSC Ensembl
Innerchr16:14796084..14971206hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38175123
hg19175123
hg18175123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046737
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557539
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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