A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524088



Internal ID15451381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73296475..73404993hg38UCSC Ensembl
Innerchr18:70963710..71072228hg19UCSC Ensembl
Innerchr18:69114690..69223208hg18UCSC Ensembl
Innerchr18:69114690..69223208hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38108519
hg19108519
hg18108519
hg17108519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699960
Samples
Known GenesLOC100505817
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524088
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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