A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4874n100



Internal ID22790961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130041779..130133008hg38UCSC Ensembl
chr3:129760622..129851851hg19UCSC Ensembl
chr3:131243312..131334541hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3891230
hg1991230
hg1891230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013275, nsv998488, nsv998586, nsv1004145, nsv1012622, nsv1013509, nsv1008653, nsv998546, nsv1012101, nsv1013853
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4874n100
Frequency
Sample Size11257
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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