A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027535



Internal ID19116754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20648866..20756153hg38UCSC Ensembl
Innerchr8:20506377..20613664hg19UCSC Ensembl
Innerchr8:20550657..20657944hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38107288
hg19107288
hg18107288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760479
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)nsv1027535
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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