A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7388n100



Internal ID20159004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6542253..6874231hg38UCSC Ensembl
chr9:6542253..6874231hg19UCSC Ensembl
chr9:6532253..6864231hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38331979
hg19331979
hg18331979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028402, nsv1018308, nsv1015462
Samples
Known GenesGLDC, KDM4C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7388n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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