A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2745n100



Internal ID22788832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14794726..15000839hg38UCSC Ensembl
chr16:14888583..15094696hg19UCSC Ensembl
chr16:14796084..15002197hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38206114
hg19206114
hg18206114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035310, nsv1042329, nsv1041959, nsv1044739
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)dgv2745n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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