A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5199n100



Internal ID22791286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44963167..45015559hg38UCSC Ensembl
chr4:44965184..45017576hg19UCSC Ensembl
chr4:44659941..44712333hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3852393
hg1952393
hg1852393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005919, nsv998011, nsv1009747, nsv1002121, nsv1004845, nsv1013463, nsv1005217, nsv1007329, nsv1001880, nsv1005572
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)dgv5199n100
Frequency
Sample Size11257
Observed Gain54
Observed Loss0
Observed Complex0
Frequencyn/a


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