A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3838n100



Internal ID22789925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:52731184..52942479hg38UCSC Ensembl
chr2:52958322..53169617hg19UCSC Ensembl
chr2:52811826..53023121hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38211296
hg19211296
hg18211296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014068, nsv1006244
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)dgv3838n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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