A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4920n100



Internal ID20156536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151784289..151830691hg38UCSC Ensembl
chr3:151502077..151548479hg19UCSC Ensembl
chr3:152984767..153031169hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3846403
hg1946403
hg1846403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000747, nsv1013203, nsv1007788, nsv1005945, nsv1005486, nsv1004123
Samples
Known GenesAADAC, LOC201651, MIR548H2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4920n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss58
Observed Complex0
Frequencyn/a


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