A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2782n100



Internal ID20154398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18148857..18768126hg38UCSC Ensembl
chr16:18242714..18779448hg19UCSC Ensembl
chr16:18150215..18686949hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38619270
hg19536735
hg18536735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054336, nsv1045342, nsv1047931, nsv1037716, nsv1050716, nsv1042038, nsv1050435, nsv1052170
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2782n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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