A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4906n100



Internal ID22790993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137936746..137975682hg38UCSC Ensembl
chr3:137655588..137694524hg19UCSC Ensembl
chr3:139138278..139177214hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3838937
hg1938937
hg1838937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014192, nsv1001241
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)dgv4906n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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