A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2695n100



Internal ID20154311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3347901..3424504hg38UCSC Ensembl
chr16:3397901..3474504hg19UCSC Ensembl
chr16:3337902..3414505hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3876604
hg1976604
hg1876604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045434, nsv1045995
Samples
Known GenesMTRNR2L4, OR2C1, ZNF174, ZSCAN32
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2695n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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