A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7687n100



Internal ID19018055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90836574..90936821hg38UCSC Ensembl
chr9:93598856..93699103hg19UCSC Ensembl
chr9:92638677..92738924hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38100248
hg19100248
hg18100248
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039761, nsv1053252, nsv1039326
Samples
Known GenesSYK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7687n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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