A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4799n100



Internal ID22790886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80531712..80563946hg38UCSC Ensembl
chr3:80580862..80613096hg19UCSC Ensembl
chr3:80663552..80695786hg18UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg3832235
hg1932235
hg1832235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002321, nsv1012779
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)dgv4799n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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