A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7184n100



Internal ID22793271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40326266..40344169hg38UCSC Ensembl
chr8:40183785..40201688hg19UCSC Ensembl
chr8:40302942..40320845hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3817904
hg1917904
hg1817904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029594, nsv1019818, nsv1019020, nsv1020785, nsv1034522
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)dgv7184n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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