A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4716n100



Internal ID22790803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35445121..35552716hg38UCSC Ensembl
chr3:35486613..35594208hg19UCSC Ensembl
chr3:35461617..35569212hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38107596
hg19107596
hg18107596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009907, nsv997561, nsv1007679
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)dgv4716n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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