A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4563n100



Internal ID20156179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36142329..36186502hg38UCSC Ensembl
chr22:36538377..36582550hg19UCSC Ensembl
chr22:34868323..34912496hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3844174
hg1944174
hg1844174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065631, nsv1058476
Samples
Known GenesAPOL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4563n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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