A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4830n100



Internal ID20156446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100605431..100729339hg38UCSC Ensembl
chr3:100324275..100448183hg19UCSC Ensembl
chr3:101806965..101930873hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38123909
hg19123909
hg18123909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007437, nsv1006559, nsv1008949, nsv1006303, nsv1005065, nsv1008353, nsv999432, nsv1002624, nsv1014117, nsv1007742, nsv1006373, nsv1009835, nsv1006402, nsv1007046
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4830n100
Frequency
Sample Size29084
Observed Gain127
Observed Loss0
Observed Complex0
Frequencyn/a


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