A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4841n100



Internal ID22790928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113845386..113904192hg38UCSC Ensembl
chr3:113564233..113623039hg19UCSC Ensembl
chr3:115046923..115105729hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3858807
hg1958807
hg1858807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012691, nsv1012224, nsv1007690, nsv1010004, nsv1012955
Samples
Known GenesGRAMD1C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4841n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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