A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518471



Internal ID15099078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:39432744..39706408hg38UCSC Ensembl
Innerchr18:37012708..37286372hg19UCSC Ensembl
Innerchr18:35266706..35540370hg18UCSC Ensembl
Innerchr18:35266706..35540370hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38273665
hg19273665
hg18273665
hg17273665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695907
Samples
Known GenesLINC00669, MIR5583-1, MIR5583-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518471
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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