A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7233n100



Internal ID22793320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60076796..60097061hg38UCSC Ensembl
chr8:60989355..61009620hg19UCSC Ensembl
chr8:61151909..61172174hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3820266
hg1920266
hg1820266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015316, nsv1028809, nsv1031967, nsv1033495, nsv1027485
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)dgv7233n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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