A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv14n21



Internal ID20131735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103374133..103586151hg38UCSC Ensembl
chr1:103916755..104128773hg19UCSC Ensembl
chr1:103689343..103930296hg18UCSC Ensembl
chr1:103628776..103840794hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38212019
hg19212019
hg18240954
hg17212019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527283, nsv527940
Samples
Known GenesACTG1P4, AMY2B, LOC101928436, RNPC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv14n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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