A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv319n21



Internal ID22766511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38464035..38537676hg38UCSC Ensembl
chr4:38465656..38539297hg19UCSC Ensembl
chr4:38142051..38215692hg18UCSC Ensembl
chr4:38288222..38361863hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3873642
hg1973642
hg1873642
hg1773642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527181, nsv524517
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv319n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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