A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5742n100



Internal ID22791829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:101580851..101949666hg38UCSC Ensembl
chr5:100916555..101285370hg19UCSC Ensembl
chr5:100944454..101313269hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38368816
hg19368816
hg18368816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028227, nsv1020503, nsv1026660, nsv1023748, nsv1020197
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)dgv5742n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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