A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7723n100



Internal ID20159339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134309226..134469090hg38UCSC Ensembl
chr9:137201072..137360936hg19UCSC Ensembl
chr9:136340893..136500757hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38159865
hg19159865
hg18159865
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042127, nsv1040005, nsv1051221, nsv1053174, nsv1047987
Samples
Known GenesMIR4669, RXRA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7723n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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