A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7325n100



Internal ID22793412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136660521..136858422hg38UCSC Ensembl
chr8:137672764..137870665hg19UCSC Ensembl
chr8:137741946..137939847hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38197902
hg19197902
hg18197902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015463, nsv1018249, nsv1034672, nsv1022076, nsv1018016, nsv1034655, nsv1017999, nsv1016479, nsv1024457, nsv1016386, nsv1033512, nsv1025348, nsv1030971, nsv1024232, nsv1032154, nsv1029640, nsv1021631, nsv1032623, nsv1029556, nsv1028653, nsv1029426, nsv1031439, nsv1021493, nsv1016647, nsv1019151, nsv1021751, nsv1028255, nsv1033514, nsv1027239, nsv1027565
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)dgv7325n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss415
Observed Complex0
Frequencyn/a


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