A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518311



Internal ID15445604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18486532..18486951hg38UCSC Ensembl
Innerchr1:18813026..18813445hg19UCSC Ensembl
Innerchr1:18685613..18686032hg18UCSC Ensembl
Innerchr1:18558332..18558751hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38420
hg19420
hg18420
hg17420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695742
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518311
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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