A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7542n100



Internal ID22793629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39445501..39990996hg38UCSC Ensembl
chr9:41475094..42136014hg19UCSC Ensembl
chr9:41465094..42126014hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38545496
hg19660921
hg18660921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034224, nsv1022243, nsv1029216
Samples
Known GenesKGFLP2, LOC643648, LOC653501, MGC21881, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7542n100
Frequency
Sample Size11257
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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