A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4432n100



Internal ID22790519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38742206..38789148hg38UCSC Ensembl
chr21:40114130..40161072hg19UCSC Ensembl
chr21:39036000..39082942hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3846943
hg1946943
hg1846943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060535, nsv1063936, nsv1055623, nsv1057627
Samples
Known GenesLINC00114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4432n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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