A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4097n100



Internal ID20155713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161429698..161480024hg38UCSC Ensembl
chr2:162286209..162336535hg19UCSC Ensembl
chr2:161994455..162044781hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3850327
hg1950327
hg1850327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999728, nsv1011325
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)dgv4097n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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