A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041959



Internal ID19131178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..14979089hg38UCSC Ensembl
Innerchr16:14888583..15072946hg19UCSC Ensembl
Innerchr16:14796084..14980447hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38184364
hg19184364
hg18184364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2745n100
Supporting Variantsnssv3557541
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)nsv1041959
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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