A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3741n100



Internal ID22789828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23748491..23857418hg38UCSC Ensembl
chr2:23971361..24080288hg19UCSC Ensembl
chr2:23824865..23933792hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38108928
hg19108928
hg18108928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014398, nsv1000013, nsv1000157, nsv1014412
Samples
Known GenesATAD2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3741n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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