A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4425n100



Internal ID22790512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32037619..32098317hg38UCSC Ensembl
chr21:33409932..33470630hg19UCSC Ensembl
chr21:32331803..32392501hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3860699
hg1960699
hg1860699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066591, nsv1056554, nsv1066380, nsv1066624
Samples
Known GenesLINC00159
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4425n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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