A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3141n100



Internal ID19013509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33630132..34611003hg38UCSC Ensembl
chr17:31957151..32938022hg19UCSC Ensembl
chr17:28981264..29962135hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38980872
hg19980872
hg18980872
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066757, nsv1061741, nsv1064104
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3141n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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