A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2752n100



Internal ID20154368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14869830..15022388hg38UCSC Ensembl
chr16:14963687..15116245hg19UCSC Ensembl
chr16:14871188..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38152559
hg19152559
hg18152559
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038785, nsv1035526, nsv1038020, nsv1042275, nsv1055110
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)dgv2752n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss61
Observed Complex0
Frequencyn/a


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