A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4925n100



Internal ID22791012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154571387..154727150hg38UCSC Ensembl
chr3:154289176..154444939hg19UCSC Ensembl
chr3:155771870..155927633hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38155764
hg19155764
hg18155764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998101, nsv1007902
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4925n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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