A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv119n21



Internal ID22766311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108331662..108339325hg38UCSC Ensembl
chr13:108984010..108991673hg19UCSC Ensembl
chr13:107782011..107789674hg18UCSC Ensembl
chr13:107782011..107789674hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg387664
hg197664
hg187664
hg177664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519175, nsv527316
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv119n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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