A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4704n100



Internal ID22790791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25235837..25285744hg38UCSC Ensembl
chr3:25277328..25327235hg19UCSC Ensembl
chr3:25252332..25302239hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3849908
hg1949908
hg1849908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006455, nsv1012646
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)dgv4704n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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