A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4703n100



Internal ID22790790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24882828..24901114hg38UCSC Ensembl
chr3:24924319..24942605hg19UCSC Ensembl
chr3:24899323..24917609hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3818287
hg1918287
hg1818287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012430, nsv1002800
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)dgv4703n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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