A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3297n100



Internal ID20154913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82879855..83048753hg38UCSC Ensembl
chr17:80837731..81006629hg19UCSC Ensembl
chr17:78431020..78599918hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38168899
hg19168899
hg18168899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064259, nsv1055735
Samples
Known GenesB3GNTL1, TBCD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3297n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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