A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4821n100



Internal ID22790908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99136225..99234905hg38UCSC Ensembl
chr3:98855069..98953749hg19UCSC Ensembl
chr3:100337759..100436439hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3898681
hg1998681
hg1898681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004438, nsv1014277, nsv998521, nsv1012264, nsv1008663, nsv997372, nsv1000298
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)dgv4821n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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