A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2777n100



Internal ID20154393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16236621..16695080hg38UCSC Ensembl
chr16:16330478..16788937hg19UCSC Ensembl
chr16:16237979..16696438hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38458460
hg19458460
hg18458460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043761, nsv1037128, nsv1040533, nsv1047879, nsv1038838
Samples
Known GenesLOC100288162, 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)dgv2777n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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