A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7474n100



Internal ID20159090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21171268..21228249hg38UCSC Ensembl
chr9:21171267..21228248hg19UCSC Ensembl
chr9:21161267..21218248hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3856982
hg1956982
hg1856982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022579, nsv1018561, nsv1016978
Samples
Known GenesIFNA10, IFNA16, IFNA17, IFNA4, IFNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7474n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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