A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3145n100



Internal ID19013513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36097969..36258784hg38UCSC Ensembl
chr17:34425363..34586282hg19UCSC Ensembl
chr17:31449476..31610395hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38160816
hg19160920
hg18160920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056011, nsv1064321, nsv1065458, nsv1064855, nsv1062384, nsv1056091, nsv1058034, nsv1058575, nsv1066981, nsv1058811, nsv1061275, nsv1065224, nsv1064894
Samples
Known GenesCCL3L1, CCL3L3, CCL4, CCL4L1, CCL4L2, TBC1D3B, TBC1D3H
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3145n100
Frequency
Sample Size29084
Observed Gain117
Observed Loss0
Observed Complex0
Frequencyn/a


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