A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522681



Internal ID15449974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89681893..89709750hg38UCSC Ensembl
Innerchr4:90603044..90630901hg19UCSC Ensembl
Innerchr4:90822067..90849924hg18UCSC Ensembl
Innerchr4:90960222..90988079hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3827858
hg1927858
hg1827858
hg1727858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706089
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522681
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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