A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020787



Internal ID19110005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89424847..89491908hg38UCSC Ensembl
Innerchr8:90437076..90504137hg19UCSC Ensembl
Innerchr8:90506192..90573253hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3867062
hg1967062
hg1867062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689699
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)nsv1020787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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