A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2740n100



Internal ID19013108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14683524..14986586hg38UCSC Ensembl
chr16:14777381..15080443hg19UCSC Ensembl
chr16:14684882..14987944hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38303063
hg19303063
hg18303063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052126, nsv1037993, nsv1037627
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, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2740n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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