A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526544



Internal ID15453837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:97731435..97752565hg38UCSC Ensembl
Innerchr8:98743663..98764793hg19UCSC Ensembl
Innerchr8:98812839..98833969hg18UCSC Ensembl
Innerchr8:98812839..98833969hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3821131
hg1921131
hg1821131
hg1721131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702858
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526544
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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