A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2776n100



Internal ID20154392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16200849..16704794hg38UCSC Ensembl
chr16:16294706..16798651hg19UCSC Ensembl
chr16:16202207..16706152hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38503946
hg19503946
hg18503946
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047549, nsv1035531, nsv1048626, nsv1035149, nsv1036919, nsv1039247, nsv1044473, nsv1050063
Samples
Known GenesABCC6, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO3, NPIPA7, NPIPA8, PKD1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2776n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss13
Observed Complex0
Frequencyn/a


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