A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5456n100



Internal ID22791543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161025216..161108645hg38UCSC Ensembl
chr4:161946368..162029797hg19UCSC Ensembl
chr4:162165818..162249247hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3883430
hg1983430
hg1883430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034718, nsv1031209, nsv1020541
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)dgv5456n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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