A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7716n100



Internal ID22793803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125985970..126072015hg38UCSC Ensembl
chr9:128748249..128834294hg19UCSC Ensembl
chr9:127788070..127874115hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3886046
hg1986046
hg1886046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046564, nsv1052329, nsv1041510
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)dgv7716n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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