A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7681n100



Internal ID22793768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77148171..77175939hg38UCSC Ensembl
chr9:79763087..79790855hg19UCSC Ensembl
chr9:78952907..78980675hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3827769
hg1927769
hg1827769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043527, nsv1044134, nsv1038763
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)dgv7681n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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