A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3156n100



Internal ID20154772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36589879..36646211hg38UCSC Ensembl
chr17:34946309..35002667hg19UCSC Ensembl
chr17:32020422..32076780hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3856333
hg1956359
hg1856359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058933, nsv1060317
Samples
Known GenesDHRS11, MRM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3156n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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