A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3714n100



Internal ID22789801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9890835..9925495hg38UCSC Ensembl
chr2:10030964..10065624hg19UCSC Ensembl
chr2:9948415..9983075hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3834661
hg1934661
hg1834661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006533, nsv1004743
Samples
Known GenesTAF1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3714n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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