A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4831n100



Internal ID20156447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100621212..100709093hg38UCSC Ensembl
chr3:100340056..100427937hg19UCSC Ensembl
chr3:101822746..101910627hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3887882
hg1987882
hg1887882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002525, nsv1013021, nsv1006045, nsv1004887, nsv1009705, nsv1009944, nsv1004273, nsv1008743, nsv1005369
Samples
Known GenesGPR128
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4831n100
Frequency
Sample Size29084
Observed Gain60
Observed Loss0
Observed Complex0
Frequencyn/a


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