A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7691n100



Internal ID22793778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102807930..102992459hg38UCSC Ensembl
chr9:105570212..105754741hg19UCSC Ensembl
chr9:104610033..104794562hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38184530
hg19184530
hg18184530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053435, nsv1054263
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)dgv7691n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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