A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2741n100



Internal ID19013109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14741198..14991815hg38UCSC Ensembl
chr16:14835055..15085672hg19UCSC Ensembl
chr16:14742556..14993173hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38250618
hg19250618
hg18250618
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043568, nsv1050778
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2741n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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