A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5197n100



Internal ID22791284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43184487..43214677hg38UCSC Ensembl
chr4:43186504..43216694hg19UCSC Ensembl
chr4:42881261..42911451hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3830191
hg1930191
hg1830191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998050, nsv1004634
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)dgv5197n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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