A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4844n100



Internal ID22790931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119000633..119115295hg38UCSC Ensembl
chr3:118719480..118834142hg19UCSC Ensembl
chr3:120202170..120316832hg18UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38114663
hg19114663
hg18114663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009337, nsv1004362, nsv1009679, nsv1003600, nsv998269, nsv1001072, nsv1003911, nsv999739, nsv997442, nsv1003674, nsv1004498, nsv1010482, nsv1004077
Samples
Known GenesIGSF11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4844n100
Frequency
Sample Size11257
Observed Gain36
Observed Loss0
Observed Complex0
Frequencyn/a


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