A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2753n100



Internal ID20154369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14869830..15034129hg38UCSC Ensembl
chr16:14963687..15127986hg19UCSC Ensembl
chr16:14871188..15035487hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38164300
hg19164300
hg18164300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050915, nsv1036772, nsv1046124, nsv1050373, nsv1044312, nsv1039484, nsv1040219
Samples
Known GenesLOC100288162, MIR1972-1, MIR1972-2, 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)dgv2753n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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