A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv329n21



Internal ID22766521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:177497947..177580762hg38UCSC Ensembl
chr4:178419101..178501916hg19UCSC Ensembl
chr4:178656095..178738910hg18UCSC Ensembl
chr4:178794250..178877065hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3882816
hg1982816
hg1882816
hg1782816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv517838, nsv524425
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv329n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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