A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2755n100



Internal ID19013123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14877546..15434384hg38UCSC Ensembl
chr16:14971403..15528241hg19UCSC Ensembl
chr16:14878904..15435742hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38556839
hg19556839
hg18556839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054731, nsv1052648
Samples
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, MPV17L, NOMO1, NPIPA1, NPIPA5, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2755n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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