A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4982n100



Internal ID20156598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167184267..167248071hg38UCSC Ensembl
chr3:166902055..166965859hg19UCSC Ensembl
chr3:168384749..168448553hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3863805
hg1963805
hg1863805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012308, nsv997378
Samples
Known GenesZBBX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4982n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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