A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4567n100



Internal ID22790654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38890960..38933588hg38UCSC Ensembl
chr22:39286965..39329593hg19UCSC Ensembl
chr22:37616911..37659539hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3842629
hg1942629
hg1842629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064509, nsv1066042
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)dgv4567n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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