A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7666n100



Internal ID20159282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68896889..69228107hg38UCSC Ensembl
chr9:71511805..71843023hg19UCSC Ensembl
chr9:70701625..71032843hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38331219
hg19331219
hg18331219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051798, nsv1050692
Samples
Known GenesFXN, PIP5K1B, PRKACG, TJP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7666n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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