A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019288



Internal ID19108506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21406467..21445678hg38UCSC Ensembl
Innerchr8:21263978..21303189hg19UCSC Ensembl
Innerchr8:21308258..21347469hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3839212
hg1939212
hg1839212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685336
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)nsv1019288
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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