A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4916n100



Internal ID22791003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145508846..145538536hg38UCSC Ensembl
chr3:145226633..145256323hg19UCSC Ensembl
chr3:146709323..146739013hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3829691
hg1929691
hg1829691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002549, nsv1001259, nsv1000430
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)dgv4916n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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