A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4472n100



Internal ID20156088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18888903..19037700hg38UCSC Ensembl
chr22:18876416..19025213hg19UCSC Ensembl
chr22:17256416..17405213hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38148798
hg19148798
hg18148798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064300, nsv1056538
Samples
Known GenesDGCR10, DGCR2, DGCR5, DGCR6, DGCR9, PRODH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4472n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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