A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7264n100



Internal ID22793351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88381589..88431163hg38UCSC Ensembl
chr8:89393818..89443392hg19UCSC Ensembl
chr8:89462934..89512508hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3849575
hg1949575
hg1849575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019671, nsv1029978
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)dgv7264n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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