A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4390n100



Internal ID20156006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15582251..15773439hg38UCSC Ensembl
chr21:16954570..17145758hg19UCSC Ensembl
chr21:15876441..16067629hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38191189
hg19191189
hg18191189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059500, nsv1064683
Samples
Known GenesUSP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4390n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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