A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521302



Internal ID15448595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:70437354..70493338hg38UCSC Ensembl
Innerchr18:68104590..68160574hg19UCSC Ensembl
Innerchr18:66255570..66311554hg18UCSC Ensembl
Innerchr18:66255570..66311554hg17UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3855985
hg1955985
hg1855985
hg1755985
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697908
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521302
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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