A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042774



Internal ID18785305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14662418..15031584hg38UCSC Ensembl
Innerchr16:14756275..15125441hg19UCSC Ensembl
Innerchr16:14663776..15032942hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38369167
hg19369167
hg18369167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2738n100
Supporting Variantsnssv3557236
Samples
Known GenesABCC6P2, BFAR, LOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PDXDC1, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042774
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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