A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv19n21



Internal ID20131740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179792466..179826370hg38UCSC Ensembl
chr1:179761601..179795505hg19UCSC Ensembl
chr1:178028224..178062128hg18UCSC Ensembl
chr1:176493258..176527162hg17UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3833905
hg1933905
hg1833905
hg1733905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520418, nsv519307
Samples
Known GenesFAM163A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv19n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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