A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7684n100



Internal ID22793771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78823623..78859088hg38UCSC Ensembl
chr9:81438539..81474004hg19UCSC Ensembl
chr9:80628359..80663824hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3835466
hg1935466
hg1835466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036198, nsv1053079
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)dgv7684n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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