A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4651n100



Internal ID22790738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4099559..4172280hg38UCSC Ensembl
chr3:4141243..4213964hg19UCSC Ensembl
chr3:4116243..4188964hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3872722
hg1972722
hg1872722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012489, nsv1010014, nsv1006386, nsv1004310, nsv1010233, nsv1012735
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)dgv4651n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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