A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7722n100



Internal ID20159338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134261330..134467038hg38UCSC Ensembl
chr9:137153176..137358884hg19UCSC Ensembl
chr9:136292997..136498705hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38205709
hg19205709
hg18205709
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054219, nsv1049029, nsv1051231, nsv1049652, nsv1046242, nsv1041625, nsv1038170
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)dgv7722n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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