A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523827



Internal ID15451120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11550892..11628711hg38UCSC Ensembl
Innerchr8:11408401..11486220hg19UCSC Ensembl
Innerchr8:11445810..11523629hg18UCSC Ensembl
Innerchr8:11445810..11523629hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3877820
hg1977820
hg1877820
hg1777820
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699658
Samples
Known GenesBLK, LINC00208
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523827
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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