A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5772n100



Internal ID22791859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106778097..106811381hg38UCSC Ensembl
chr5:106113798..106147082hg19UCSC Ensembl
chr5:106141697..106174981hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3833285
hg1933285
hg1833285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026307, nsv1015781
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)dgv5772n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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