A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051228



Internal ID18793759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..14986586hg38UCSC Ensembl
Innerchr16:14888583..15080443hg19UCSC Ensembl
Innerchr16:14796084..14987944hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38191861
hg19191861
hg18191861
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2746n100
Supporting Variantsnssv3557543, nssv3557542
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051228
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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