A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7721n100



Internal ID22793808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133664644..133753192hg38UCSC Ensembl
chr9:136529766..136618314hg19UCSC Ensembl
chr9:135519587..135608135hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3888549
hg1988549
hg1888549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049281, nsv1049434
Samples
Known GenesSARDH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7721n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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