A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2744n100



Internal ID22788831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14794726..14993308hg38UCSC Ensembl
chr16:14888583..15087165hg19UCSC Ensembl
chr16:14796084..14994666hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38198583
hg19198583
hg18198583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052916, nsv1045922, nsv1046586, nsv1049917, nsv1040301, nsv1037498, nsv1044179
Samples
Known GenesABCC6P2, LOC100288162, 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)dgv2744n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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