A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4822n100



Internal ID22790909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99170132..99234905hg38UCSC Ensembl
chr3:98888976..98953749hg19UCSC Ensembl
chr3:100371666..100436439hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3864774
hg1964774
hg1864774
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004810, nsv1011995, nsv1014172, nsv1010851, nsv1010759, nsv1003886, nsv1010512
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)dgv4822n100
Frequency
Sample Size11257
Observed Gain54
Observed Loss0
Observed Complex0
Frequencyn/a


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