A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524533



Internal ID15451826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11670846..11683432hg38UCSC Ensembl
Innerchr18:11670845..11683431hg19UCSC Ensembl
Innerchr18:11660845..11673431hg18UCSC Ensembl
Innerchr18:11660845..11673431hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3812587
hg1912587
hg1812587
hg1712587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700483
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524533
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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