A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv267n21



Internal ID20131988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:227352..228838hg38UCSC Ensembl
chr3:269035..270521hg19UCSC Ensembl
chr3:244035..245521hg18UCSC Ensembl
chr3:244035..245521hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg381487
hg191487
hg181487
hg171487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv520115, nsv526216
Samples
Known GenesCHL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv267n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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