A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7574n100



Internal ID22793661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42697890..42856259hg38UCSC Ensembl
chr9:44114860..44273229hg19UCSC Ensembl
chr9:44054856..44213225hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38158370
hg19158370
hg18158370
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018117, nsv1028101
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7574n100
Frequency
Sample Size11257
Observed Gain10
Observed Loss3
Observed Complex0
Frequencyn/a


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