A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5379n100



Internal ID22791466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121404899..121495660hg38UCSC Ensembl
chr4:122326054..122416815hg19UCSC Ensembl
chr4:122545504..122636265hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3890762
hg1990762
hg1890762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008355, nsv1008501, nsv1008337, nsv997667, nsv997266, nsv997988, nsv1007392
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5379n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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