A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4649n100



Internal ID20156265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4073038..4120843hg38UCSC Ensembl
chr3:4114722..4162527hg19UCSC Ensembl
chr3:4089722..4137527hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3847806
hg1947806
hg1847806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008408, nsv998464, nsv1011840, nsv997706
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)dgv4649n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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