A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4096n100



Internal ID20155712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159097908..159201276hg38UCSC Ensembl
chr2:159954420..160057787hg19UCSC Ensembl
chr2:159662666..159766033hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38103369
hg19103368
hg18103368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001404, nsv998376
Samples
Known GenesMIR6888, TANC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4096n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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