A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525562



Internal ID15452855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42169598..42220928hg38UCSC Ensembl
Innerchr18:39749562..39800893hg19UCSC Ensembl
Innerchr18:38003560..38054891hg18UCSC Ensembl
Innerchr18:38003560..38054891hg17UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3851331
hg1951332
hg1851332
hg1751332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701701
Samples
Known GenesLINC00907
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525562
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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