A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7695n100



Internal ID22793782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104042528..104090136hg38UCSC Ensembl
chr9:106804809..106852417hg19UCSC Ensembl
chr9:105844630..105892238hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3847609
hg1947609
hg1847609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047242, nsv1051839, nsv1047060, nsv1051220, nsv1035258, nsv1039801, nsv1052813
Samples
Known GenesMIR6130
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7695n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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