A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2738n100



Internal ID19013106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14617525..15031584hg38UCSC Ensembl
chr16:14711382..15125441hg19UCSC Ensembl
chr16:14618883..15032942hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38414060
hg19414060
hg18414060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040576, nsv1054535, nsv1043497, nsv1050689, nsv1042774, nsv1037352, nsv1044868, nsv1039689, nsv1050319, nsv1050926, nsv1038390, nsv1036690, nsv1043202, nsv1040272
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, PARN, 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)dgv2738n100
Frequency
Sample Size29084
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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