A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4904n100



Internal ID22790991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:137309100..137324366hg38UCSC Ensembl
chr3:137027942..137043208hg19UCSC Ensembl
chr3:138510632..138525898hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3815267
hg1915267
hg1815267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007692, nsv997684, nsv1014492
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)dgv4904n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss63
Observed Complex0
Frequencyn/a


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