A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036093



Internal ID18778624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14741198..14993308hg38UCSC Ensembl
Innerchr16:14835055..15087165hg19UCSC Ensembl
Innerchr16:14742556..14994666hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38252111
hg19252111
hg18252111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2742n100
Supporting Variantsnssv3557529, nssv3557530
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036093
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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