A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557254



Internal ID18508849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14741198..14983611hg38UCSC Ensembl
Innerchr16:14835055..15077468hg19UCSC Ensembl
Innerchr16:14742556..14984969hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38242414
hg19242414
hg18242414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040978
Supporting Variants
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)nssv3557254
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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