A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7704n100



Internal ID20159320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113092059..113122780hg38UCSC Ensembl
chr9:115854339..115885060hg19UCSC Ensembl
chr9:114894160..114924881hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3830722
hg1930722
hg1830722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040513, nsv1046217, nsv1042807
Samples
Known GenesFAM225A, FAM225B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7704n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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