A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5391n100



Internal ID22791478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:131587715..131631063hg38UCSC Ensembl
chr4:132508870..132552218hg19UCSC Ensembl
chr4:132728320..132771668hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3843349
hg1943349
hg1843349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033412, nsv1032229, nsv1019390, nsv1034738, nsv1029489, nsv1016565, nsv1027946, nsv1016741
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)dgv5391n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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