A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522894



Internal ID15450187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:126369452..126404322hg38UCSC Ensembl
Innerchr8:127381697..127416567hg19UCSC Ensembl
Innerchr8:127450879..127485749hg18UCSC Ensembl
Innerchr8:127450879..127485749hg17UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3834871
hg1934871
hg1834871
hg1734871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698552
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522894
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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