A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv108n21



Internal ID22766300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37466130..37471028hg38UCSC Ensembl
chr13:38040267..38045165hg19UCSC Ensembl
chr13:36938267..36943165hg18UCSC Ensembl
chr13:36938267..36943165hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg384899
hg194899
hg184899
hg174899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521650, nsv519270
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv108n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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