A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv323n21



Internal ID22766515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91320436..91372331hg38UCSC Ensembl
chr4:92241587..92293482hg19UCSC Ensembl
chr4:92460610..92512505hg18UCSC Ensembl
chr4:92598765..92650660hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3851896
hg1951896
hg1851896
hg1751896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522208, nsv529020
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv323n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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