A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv134n21



Internal ID22766326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:40963145..41136353hg38UCSC Ensembl
chr14:41432350..41605556hg19UCSC Ensembl
chr14:40502100..40675306hg18UCSC Ensembl
chr14:40502100..40675306hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38173209
hg19173207
hg18173207
hg17173207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523330, nsv528301
Samples
Known GenesLOC644919
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv134n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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