A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4823n100



Internal ID22790910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99203270..99234905hg38UCSC Ensembl
chr3:98922114..98953749hg19UCSC Ensembl
chr3:100404804..100436439hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3831636
hg1931636
hg1831636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998405, nsv997394, nsv1005496, nsv1011609
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)dgv4823n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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