A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3272n100



Internal ID20154888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59564145..59685102hg38UCSC Ensembl
chr17:57641506..57762463hg19UCSC Ensembl
chr17:54996288..55117245hg18UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38120958
hg19120958
hg18120958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057033, nsv1063451
Samples
Known GenesCLTC, DHX40
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3272n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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