A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv322n21



Internal ID20132043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87811611..87812379hg38UCSC Ensembl
chr4:88732763..88733531hg19UCSC Ensembl
chr4:88951787..88952555hg18UCSC Ensembl
chr4:89089942..89090710hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38769
hg19769
hg18769
hg17769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526279, nsv527296
Samples
Known GenesIBSP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv322n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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