A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv178n21



Internal ID20131899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36084845..36153146hg38UCSC Ensembl
chr17:34412202..34480526hg19UCSC Ensembl
chr17:31436315..31504639hg18UCSC Ensembl
chr17:31436315..31504639hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3868302
hg1968325
hg1868325
hg1768325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522835, nsv524951
Samples
Known GenesCCL3, CCL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv178n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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