A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2765n100



Internal ID20154381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14954899..15322641hg38UCSC Ensembl
chr16:15048756..15416498hg19UCSC Ensembl
chr16:14956257..15323999hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38367743
hg19367743
hg18367743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036878, nsv1047178
Samples
Known GenesMIR1972-1, MIR1972-2, MIR3180-4, MIR6511B-1, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2765n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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